Penicillium Mix: Package Insert and Label Information

PENICILLIUM MIX- penicillium digitatum, penicillium camemberti, penicillium chrysogenum var. chrysogenum and penicillium roqueforti solution
PENICILLIUM MIX- penicillium camemberti, penicillium chrysogenum var. chrysogenum, penicillium roqueforti and penicillium digitatum solution
PHYCOMYCETES MIX- mucor circinelloides f. lusitanicus and rhizopus stolonifer solution
RHIZOPUS MIX- rhizopus stolonifer and rhizopus arrhizus solution
ASPERGILLUS FLAVUS- aspergillus flavus solution
BIPOLARIS SOROKINIANA- cochliobolus sativus solution
PENICILLIUM DIGITATUM- penicillium digitatum solution
MUCOR MIX- mucor circinelloides f. lusitanicus and mucor plumbeus solution
MOLD MIX 2- rhizopus stolonifer, cochliobolus spicifer, gibberella fujikuroi, aureobasidium pullulans var. pullutans and mucor plumbeus solution
ASPERGILLUS MIX- aspergillus niger var. niger, aspergillus fumigatus, eurotium amstelodami, aspergillus flavus and aspergillus nidulans solution
MONILIA MIX- candida albicans and neurospora intermedia solution
ASPERGILLUS FUMIGATUS- aspergillus fumigatus solution
AUREOBASIDIUM PULLULANS- aureobasidium pullulans var. pullutans solution
MOLD MIX 3- cladosporium sphaerospermum, aspergillus niger var. niger, alternaria alternata and penicillium chrysogenum var. chrysogenum solution
DRECHSLERA SPICIFERA- cochliobolus spicifer solution
EPIDERMOPHYTON FLOCCOSUM- epidermophyton floccosum solution
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES- mucor circinelloides f. circinelloides solution
NEUROSPORA INTERMEDIA- neurospora intermedia solution
PAECILOMYCES VARIOTII- paecilomyces variotii solution
PENICILLIUM CHRYSOGENUM (NOTATUM)- penicillium chrysogenum var. chrysogenum solution
PHOMA BETAE- pleospora betae solution
FUSARIUM MONILIFORME- gibberella fujikuroi solution
GEOTRICHUM CANDIDUM- geotrichum candidum solution
RHIZOPUS ORYZAE- rhizopus arrhizus solution
RHODOTORULA MUCILAGINOSA- rhodotorula mucilaginosa solution
SACCHAROMYCES CEREVISIAE- saccharomyces cerevisiae solution
ALTERNARIA ALTERNATA- alternaria alternata solution
GLIOCLADIUM VIRIDE- gliocladium viride solution
HELMINTHOSPORIUM SOLANI- helminthosporium solani solution
MUCOR PLUMBEUS- mucor plumbeus solution
TRICHODERMA HARZIANUM- trichoderma harzianum solution
TRICHOPHYTON MENTAGROPHYTES- trichophyton mentagrophytes solution
TRICHOPHYTON RUBRUM- trichophyton rubrum solution
TRICHOTHECIUM ROSEUM- trichothecium roseum solution
STEMPHYLIUM SOLANI- stemphylium solani solution
MUCOR CIRCINELLOIDES F. LUSITANICUS- mucor circinelloides f. lusitanicus solution
EPICOCCUM NIGRUM- epicoccum nigrum solution
MICROSPORUM CANIS- microsporum canis solution
BERMUDA GRASS SMUT- ustilago cynodontis solution
ASPERGILLUS AMSTELODAMI- eurotium amstelodami solution
ASPERGILLUS NIDULANS- aspergillus nidulans solution
ASPERGILLUS NIGER- aspergillus niger var. niger solution
BOTRYTIS CINEREA- botrytis cinerea solution
CLADOSPORIUM HERBARUM- cladosporium herbarum solution
CANDIDA ALBICANS- candida albicans solution
FUSARIUM SOLANI- haematonectria haematococca solution
CHAETOMIUM GLOBOSUM- chaetomium globosum solution
CLADOSPORIUM SPHAEROSPERMUM- cladosporium sphaerospermum solution
ALTERNARIA/HORMODENDRUM MIX- aspergillus fumigatus and alternaria alternata solution
ACREMONIUM STRICTUM- sarocladium strictum solution
NEW STOCK FUNGI MIX- rhizopus stolonifer, cochliobolus sativus, candida albicans, chaetomium globosum, trichophyton mentagrophytes, epicoccum nigrum, aspergillus niger var. niger, aureobasidium pullulans var. pullutans, gibberella fujikuroi, mucor plumbeus, alternaria alternata, acremonium strictum, botrytis cinerea, cladosporium sphaerospermum, penicillium chrysogenum var. chrysogenum and pleospora betae solution
GRAIN SMUT MIX- ustilago nuda, ustilago avenae, ustilago maydis and ustilago tritici solution
RHIZOPUS STOLONIFER- rhizopus stolonifer solution
MYCOGONE PERNICIOSA- hypomyces perniciosus solution
DEMATIACEAE MIX- cochliobolus spicifer, aureobasidium pullulans var. pullutans, cochliobolus sativus, alternaria alternata, cladosporium herbarum and helminthosporium solani solution
NEW STOCK FUNGI MIX- gibberella fujikuroi, mucor plumbeus, alternaria alternata, acremonium strictum, botrytis cinerea, cladosporium sphaerospermum, penicillium chrysogenum var. chrysogenum, pleospora betae, cochliobolus sativus, candida albicans, chaetomium globosum, rhizopus stolonifer, trichophyton mentagrophytes, aspergillus niger var. niger, aureobasidium pullulans var. pullutans and epicoccum nigrum solution
GRASS SMUT MIX- ustilago cynodontis and sporisorium cruentum solution
ALTERNARIA HORMODENDRUM MIX- alternaria alternata and aspergillus fumigatus solution
CORN SMUT- ustilago maydis solution
MOLD MIX 1- penicillium chrysogenum var. chrysogenum, aspergillus niger var. niger, cochliobolus sativus, alternaria alternata and cladosporium sphaerospermum solution
AHH MOLD MIX- cladosporium sphaerospermum, cochliobolus sativus and alternaria alternata solution
FUSARIUM MIX- haematonectria haematococca and gibberella fujikuroi solution
NEW STOCK FUNGI MIX- pleospora betae, cochliobolus sativus, candida albicans, chaetomium globosum, rhizopus stolonifer, trichophyton mentagrophytes, aspergillus niger var. niger, aureobasidium pullulans var. pullutans, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, alternaria alternata, acremonium strictum, botrytis cinerea, cladosporium sphaerospermum and penicillium chrysogenum var. chrysogenum solution
Greer Laboratories, Inc.

WARNING

THIS ALLERGENIC PRODUCT IS INTENDED FOR USE BY PHYSICIANS WHO ARE EXPERIENCED IN THE ADMINISTRATION OF ALLERGENIC EXTRACTS AND THE EMERGENCY CARE OF ANAPHYLAXIS, OR FOR USE UNDER THE GUIDANCE OF AN ALLERGY SPECIALIST.

ALLERGENIC EXTRACTS MAY CAUSE SEVERE OR FATAL ANAPHYLAXIS IN EXTREMELY SENSITIVE PATIENTS. THE INITIAL DOSE MUST BE BASED ON SKIN TESTING AS DESCRIBED IN THE DOSAGE AND ADMINISTRATION SECTION OF THIS INSERT. PATIENTS SHOULD BE INSTRUCTED TO RECOGNIZE ADVERSE REACTION SYMPTOMS AND CAUTIONED TO CONTACT THE PHYSICIAN’S OFFICE IF REACTION SYMPTOMS OCCUR. IN CERTAIN INDIVIDUALS, THESE REACTIONS COULD BE FATAL. PATIENTS SHOULD BE OBSERVED FOR AT LEAST 20 MINUTES FOLLOWING TREATMENT.

EMERGENCY MEASURES, AS WELL AS PERSONNEL TRAINED IN THEIR USE, SHOULD BE IMMEDIATELY AVAILABLE IN THE EVENT OF A LIFE‑ THREATENING REACTION. PATIENTS BEING SWITCHED FROM ONE LOT OF EXTRACT TO ANOTHER FROM THE SAME MANUFACTURER SHOULD HAVE THEIR DOSE REDUCED BY 75%.

THIS PRODUCT SHOULD NOT BE INJECTED INTRAVENOUSLY.

REFER ALSO TO THE WARNINGS, PRECAUTIONS, ADVERSE REACTIONS AND OVERDOSAGE SECTION BELOW.

Allergenic Extracts are supplied as a sterile solution for intracutaneous or subcutaneous administration. Concentrates contain the soluble extractants of the source material with 0.5% sodium chloride and 0.54% sodium bicarbonate at a pH of 6.8 to 8.4 as aqueous extracts in water for injection or in 50% glycerin. Aqueous extracts contain 0.4% phenol as a preservative and 50% glycerinated extracts contain 0.2% phenol. Diluted aqueous extracts contain Buffered Saline with 0.5% sodium chloride, 0.04% potassium phosphate, 0.11% sodium phosphate heptahydrate, and 0.4% phenol in water for injection.

Source materials for these extracts are as follows: Pollens are collected from the respective grasses, weeds, trees, shrubs, cultured plants and flowers. Mold extracts are produced from pure culture mycelial mats. Rusts and smuts are obtained from natural growths. Epidermal extracts are produced from the hide, hair, or feathers containing the natural dander, or from separated dander. Insects are the whole body insects. House dust is made from various dusts ordinarily found in the home with the extract dialyzed to remove low‑molecular weight irritants and concentrated to an extraction ratio of 1:1. Food extracts are prepared from the edible portions of the respective foods, obtained fresh if possible. Certain diagnostic food extracts contain 0.1% sodium formaldehyde sulfoxylate as an antioxidant. Other miscellaneous inhalants involved in respiratory allergy are obtained in the naturally occurring form to which a patient may be exposed.

Extracts are labeled either by weight‑to‑volume (w/v) based on the weight of the source material to the volume of the extracting fluid, or in protein nitrogen units (PNU) based on assay with one PNU representing 0.00001 mg of protein nitrogen.

The allergic reaction is dependent upon the presence of antigen‑specific immunoglobulin E (IgE) antibodies that are bound to specific receptors on mast cells and basophils. The presence of IgE antibodies on mast cells and basophils sensitizes these cells and, upon interaction with the appropriate allergen, histamine and other mediators are released. IgE antibody has been shown to correlate with atopic diseases such as allergic rhinitis and allergic asthma. (1‑4) In the skin these mediators are responsible for the characteristic wheal and flare (erythema) reactions upon Allergenic Extract skin testing in persons with the specific allergies. (3‑7)

Specific immunotherapy with Allergenic Extracts as employed for over 45 years is helpful in reducing symptoms associated with exposure to the offending allergens. A summary of effectiveness by the Panel on Review of Allergenic Extracts, an advisory committee to the U.S. Food and Drug Administration, has been published. (8) Several mechanisms have been proposed to explain the effectiveness of immunotherapy: an increase in antigen‑specific IgG antibodies is frequently associated with clinical effectiveness, although correlation is not consistent in all studies; there is a decrease in specific IgE; and IgE production is suppressed during periods of seasonal or high exposure to the antigen. (9) Other changes following immunotherapy have been noted including development of auto‑anti‑idiotypic antibodies; a decrease in blood basophil sensitivity to allergen; a decrease in lymphokine production and lymphocyte proliferation by cells exposed to allergen; and development of allergen‑specific suppressor cells. (10) The complete mechanisms of immunotherapy are not known and remain the subject of investigation.

Allergenic Extracts are indicated for the diagnosis and treatment of patients with immediate hypersensitivity allergy to the respective allergens, inhaled, ingested or otherwise introduced into contact with sensitive tissues. The diagnosis of IgE‑mediated allergy may be established by the allergy history, clinical evaluation, and skin test reactivity. (4,7,11) Immunotherapy with Allergenic Extracts is indicated when testing and patient history have identified the offending allergens and when it is not possible or practical to avoid these allergens. (12‑14) Food extracts have not been proven effective in immunotherapy.

The use of Allergenic Extracts for the above purposes should be made only by physicians with special familiarity and knowledge of allergy. (See DOSAGE AND ADMINISTRATION)

There are no known absolute contraindications to the use of Allergenic Extracts for immunotherapy. Immunotherapy with specific antigens should not be done in those individuals who do not exhibit skin test or clinical sensitivity to the particular antigens. (See below under WARNINGS and PRECAUTIONS)

Allergenic extract injections should not be administered in the presence of diseases characterized by a bleeding diathesis.

Children with nephrotic syndrome require careful consideration and probably should not receive injection therapy because a variety of seemingly unrelated events, such as immunization, can cause an exacerbation of their nephrotic disease.

General contraindications include:

EXTREME SENSITIVITY TO THE SPECIFIC ALLERGEN ‑ Determined from previous anaphylaxis following exposure.

AUTOIMMUNE DISEASE ‑ Individuals with autoimmune disease may be at risk, due to the possibility of routine immunizations exacerbating symptoms of the underlying disease.

Concentrated extracts must be diluted with a sterile diluent prior to first use on a patient for treatment or intradermal testing. Allergenic Extracts are manufactured to assure high potency and have the ability during skin testing and immunotherapy to cause serious local and systemic reactions including death in sensitive patients. Most reactions occur within 20 minutes after injection, (15) but may occur later. (16) To minimize the potential for local or systemic reactions, the relative sensitivity of the patient must be assessed from the allergic history and from clinical observations. Patients should be informed of these risks prior to skin testing and immunotherapy (see PRECAUTIONS and ADVERSE REACTIONS below).

Allergenic Extract immunotherapy doses should be lowered or temporarily withheld from patients if any of the following conditions exist:

(1) severe symptoms of rhinitis and/or asthma

(2) infection or flu accompanied by fever

(3) exposure to excessive amounts of clinically relevant allergen prior to a scheduled injection

(4) evidence of a local or systemic reaction to the preceding extract injection during a course of immunotherapy

The dosage must be reduced when modifying dosages or components in a mixture or an individual prescription, or when starting a patient on fresh extract, even though the labeled strength of the old and new vials may be the same. This reduction in dosage may be necessary due to the older vial losing potency during storage, or due to different sensitivities to different components. The amount of new extract given should not exceed 25% of the last dose given from the old vial, assuming both extracts contain comparable amounts of allergen. Any evidence of a local or generalized reaction requires a reduction in dosage during the initial stages of immunotherapy, as well as during maintenance therapy.

GENERAL:

Not for intravenous use!

Systemic allergic reactions may occur as a result of immunotherapy. The risk can be minimized by adherence to a careful injection schedule, which starts with a low concentration of extract and is increased slowly. Because of the danger of serious reactions, caution is needed in testing exquisitely sensitive patients, particularly with potent allergens, e.g., peanut, cottonseed, and flaxseed. (8) Such extracts should be appropriately diluted before use.

The physician must be prepared to treat anaphylaxis should it occur and have the necessary drugs and equipment on hand to do so. (17‑18) Extracts should not be administered by the patient or other individuals who are not prepared to treat anaphylaxis should it occur.

Patients receiving Allergenic Extracts should be kept under observation a minimum of twenty (20) minutes so that any adverse reaction can be observed and properly handled. (15) This time should be extended for high‑risk patients such as those with unstable asthma or those suffering an exacerbation of their symptoms.

Patients receiving beta blockers may not be responsive to beta adrenergic drugs used to treat anaphylaxis. The risks of anaphylaxis in these patients should be carefully weighed against the benefits of immunotherapy.

Check the lot number and dosage schedule of the patient to verify correctness of a prescription number, a vial number, or strength. Only after this verification has been made should an injection be given.

A separate sterile needle and syringe should be used for each patient to prevent transmission of hepatitis or other infectious agents.

INFORMATION FOR PATIENTS:

Most serious reactions following the administration of Allergenic Extracts occur within 20 minutes; the patient should remain under observation for this period of time or longer if instructed by the physician. The size of any local reaction should be recorded, because increasingly large local reactions may precede a subsequent systemic reaction with increasing dosage. The patient should be instructed to report any unusual reactions. In particular, this includes unusual swelling and/or tenderness at the injection site, or reactions such as rhinorrhea, sneezing, coughing, wheezing, shortness of breath, nausea, dizziness, or faintness. Reactions may occur some time after leaving the physician’s office, in which case medical attention should be sought immediately.

DRUG INTERACTIONS: Skin test diagnosis with Allergenic Extracts is contraindicated within 24 hours after the last dose of most antihistamines, within 48 hours after the last dose of terfenadine, and within 3 weeks or longer after the last dose of astemizole. These products suppress histamine skin test reactions and could mask a positive response.

CARCINOGENESIS, MUTAGENESIS, IMPAIRMENT OF FERTILITY: There is no evidence of carcinogenicity, mutagenesis or impairment of fertility in humans from Allergenic Extracts. No long‑term studies in animals have been performed to evaluate carcinogenic potential.

PREGNANCY: PREGNANCY CATEGORY C ‑ Animal reproduction studies have not been conducted with Allergenic Extracts. It is also not known whether Allergenic Extracts can cause fetal harm when administered to a pregnant woman or whether they can affect reproduction capacity. Allergenic Extracts should be given to a pregnant woman only if clearly needed.

There is no evidence of adverse effects of Allergenic Extracts on the fetus. (8) Studies have not been performed in animals to determine whether extracts affect fertility in males or females, have teratogenic potential, or have other adverse effects on the fetus. Caution should be exercised in testing or treating pregnant females because a systemic reaction may cause an abortion as a result of uterine muscle contractions.

LABOR AND DELIVERY: There is no known information of adverse effects during labor and delivery.

NURSING MOTHERS: It is not known whether this product is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when extracts are administered to a nursing woman.

PEDIATRIC AND GERIATRIC USE: Although most extracts have not been studied systematically in children, children and geriatric patients appear to tolerate injections of Allergenic Extracts well. Studies with pollenosis and asthma have been conducted in children (e.g. refs. 19‑21). Extract usage in children should follow the same precautions as in adults.

Adverse systemic reactions may occur within minutes upon use of an Allergenic Extract to which a person has specific sensitivity. These reactions consist primarily of allergic symptoms such as generalized skin erythema, urticaria, pruritus, angioedema, rhinitis, wheezing, laryngeal edema, and hypotension. Less commonly, nausea, emesis, abdominal cramps, diarrhea and uterine contractions may occur. Severe reactions may cause shock and loss of consciousness. Fatalities have occurred rarely. (8,22,23) These systemic reactions occur with varying frequency in different clinics and are usually less than 1%. To some extent, the reaction rate is related to the type and dose of administered extract and to the sensitivity of the patient. In general, immunotherapy with Allergenic Extracts is considered to be safe. (24) Despite all precautions, occasional reactions are unavoidable.

Adverse systemic reactions should be treated as follows:

A. A tourniquet should be immediately applied to the extremity above the site of injection. Release the tourniquet every few minutes for a few seconds.

B. Epinephrine 1:1000 should be injected immediately in the opposite arm in amounts of 0.3 to 0.5 mL and 0.2 mL epinephrine should be administered at the site of injection. For children below the age of 6 years, adjust the dosage of epinephrine to 0.005 mL per pound of body weight per dose. Repeat epinephrine dosage in 15 minutes if necessary and if symptoms persist.

C. Adverse reactions not responding to epinephrine therapy may require the use of parenteral bronchodilators, vasopressors, oxygen, or volume replacement therapy.

Local reactions consisting of erythema, itching, swelling, tenderness and sometimes pain may occur at the injection site. These reactions may appear within a few minutes to hours and persist for several days. Local cold applications and oral antihistamines may be effective treatment. For marked and prolonged local reactions, steroids may be helpful.

Systemic reactions are uncommon after injection, but if the patient receives more extract than can be tolerated at that particular time and begins to experience immediate hypersensitivity anaphylaxis, the procedures listed under ADVERSE REACTIONS should be instituted.

Overdosage may occur because of an error in the volume of extract injected, or an incorrect dilution injected, or because the patient may be exposed to airborne or environmental antigens simultaneously with injection of the same antigens. In the event of a systemic reaction occurring, the dosage schedule should be carefully adjusted as outlined above under WARNINGS.

1. DIAGNOSTIC TESTING

For the patient with a suspected diagnosis of allergy to more than one antigen, initial skin testing should include the individual extracts. If a screening skin test with a mixture is used, a positive response should be followed by testing with the individual extracts to determine the degree of sensitivity to each and to guide in the selection of extracts and their concentration for immunotherapy if indicated. However, because a negative skin test with a mixture may not be indicative of the absence of allergy to one or more of the components due to their dilution, testing with individual extracts is more precise. False negative responses may occur if serum levels of antihistamines remain from prior medication administration (see CONTRAINDICATIONS). The use of a positive control is especially recommended for patients on prior medications which may decrease the histamine skin test response.

Scratch or Prick‑puncture Skin Testing:

Allergenic Extract concentrates may be used for scratch or prick‑puncture testing or scratch tests in 50% glycerin, 1:20 w/v or strongest available strength in 5 mL vials may be used. Prick‑puncture tests with concentrated extracts in patients highly sensitive to the specific antigen should yield distinctive wheals with diameters of greater than 5 mm and with much larger erythema reactions. Glycerinated histamine phosphate 5 mg/mL (1.8 mg/mL histamine base) or aqueous histamine phosphate 2.75 mg/mL (1 mg/mL histamine base; 1:1,000 W/V) may be used as a positive control.

Intradermal Skin Testing:

Extract for intradermal testing must be prepared by diluting the stock concentrate injection vials with sterile diluent (use normal or buffered saline, or normal saline with human serum albumin) or the appropriate dilutions may be purchased.

a. Patients with a negative scratch or prick‑puncture test:

Patients who do not react to a scratch or prick‑puncture test should be tested intradermally, using a 26 or 27 gauge 1/4 inch needle, with 0.02 to 0.05 mL of an appropriate extract dilution from 1/100 to 1/1000 of the concentrate. A negative test should be followed by a repeat test using a higher concentration until significant wheal and flare reaction sizes are attained or until the responses remain negative. As a negative control use the diluent or, in the case of extracts in 50% glycerin, use 0.5% to 1% glycerosaline solution. As a positive control, use glycerinated histamine phosphate diluted to 0.5 mg/mL (0.18 mg/mL histamine base) or aqueous histamine phosphate 0.275 mg/mL (0.1 mg/mL histamine base).

b. Patients tested only by the intradermal method:

Since highly reactive individuals may react intracutaneously at 1:1 million or even 1:10 million dilutions, any intradermal injection should be preceded by a puncture test and the dose adjusted accordingly. Other patients suspected of being moderately allergic should be tested with 0.02 to 0.05 mL of an appropriate extract dilution on the order of 1/10,000 to 1/100,000 of the concentrate. A negative test should be followed by repeat tests using progressively stronger ten‑fold concentrations until significant wheal and flare reaction sizes are attained, or until skin test responses with the higher concentrations remain negative. As a negative control, use the diluent or, in the case of extracts in 50% glycerin, use 0.5% to 1% glycerosaline solution. As a positive control, use glycerinated histamine phosphate diluted to 0.5 mg/mL (0.18 mg/mL histamine base) or aqueous histamine phosphate 0.275 mg/mL (0.1 mg/mL histamine base).

Skin tests are graded in terms of the wheal and erythema response noted at 15 to 20 minutes, and compared to the appropriate controls. Wheal and erythema sizes may be recorded by actual measurement.

2. IMMUNOTHERAPY

Immunotherapy is administered by subcutaneous injection. Dosage of Allergenic Extracts is individualized according to the patient’s sensitivity, the clinical response, and tolerance to the extract administered during the phases of an injection regimen. The initial dose of the extract should be determined based on the puncture test reactivity. In patients who appear to be exquisitely sensitive by history and skin test, the initial dose of the extract should be 0.05 to 0.1 mL of a low concentration, such as dilution number 5 or 6 in below. Patients with lesser sensitivity may be started with 0.05 to 0.1 mL of the next higher concentration. The amount of Allergenic Extract is increased at each injection by no more than 50% of the previous amount, and the next increment is governed by the response to the last injection. Large local reactions which persist for longer than 24 hours are generally considered an indication for repeating the previous dose or reducing the dose at the next administration. Any evidence of systemic reaction is an indication for a reduction of 75% in the subsequent dose. The upper limits of dosage have not been established; however, doses larger than 0.2 mL of an extract in 50% glycerin may cause discomfort upon injection. The dosage of Allergenic Extract does not vary significantly with the allergic disease under treatment.

To prepare dilutions starting from a concentrate such as 1:10 W/V, 1:20 W/V, OR 20,000 PNU/mL, proceed as in Table 1 below. (Note: Add 0.5 mL of concentrate to 4.5 mL of sterile diluent and make additional dilutions in the same manner.)

TABLE 1

Ten-Fold Dilution Series *
*
There is no direct potency correlation across the table between PNUs and W/V.
Dilution Extract Diluent W/V W/V PNU/mL
0 Concentrate 1:10 1:20 20,000
1 0.5 mL in dilution concentrate 4.5 mL

1:100

1:200 2,000
2 0.5 mL in dilution 1 4.5 mL 1:1,000 1:2,000 200
3 0.5 mL in dilution 2 4.5 mL 1:10,000 1:20,000 20
4 0.5 mL in dilution 3 4.5 mL 1:100,000 1:200,000 2
5 0.5 mL in dilution 4 4.5 mL 1:1,000,000 1:2,000,000 0.2
6 0.5 mL in dilution 5 4.5 mL 1:10,000,000 1:20,000,000 0.0

Stock concentrate extracts containing up to 40,000 PNU/mL, or 1:10 W/V or other dilutions as requested by the physician are supplied in 5, 10, 30 and 50 mL in aqueous or 50% glycerin buffered saline. House dust extract is supplied in a 1:1 W/V concentrate, or a maximum of 10,000 PNU/mL. Extracts are also supplied in dropper vials for scratch or prick testing.

Allergenic Extracts should be stored at 2‑8°C and kept at this temperature range during office use. Refer to vial labels for expiration dates. Diluted extracts are inherently less stable than concentrates. Dilutions of glycerinated extracts which result in glycerin below 50% are also less stable. The more dilute extracts in aqueous diluents should be replenished daily. Potency of a particular dilution can be checked by skin test in comparison to a fresh dilution of the extract on an individual known to be allergic to the specific antigen.

  1. Lichtenstein LM, Ishizaka K, Norman PS, et al. IgE antibody measurements in ragweed hayfever: relationship to clinical severity and the results of immunotherapy. J Clin Invest 1973;52:474.
  2. Elgefors B, Julin A, Johansson SGO. Immunoglobulin E in bronchial asthma. Acta Allergol 1974;29:327.
  3. Norman PS. The clinical significance of IgE. Hosp Pract 1975;10:41‑49.
  4. Bryant DA, Burns MW, Lazarus L. The correlation between skin tests, bronchial provocation tests and the serum level of IgE specific for common allergens in patients with asthma. Clin Allergy 1975;5:145.
  5. Loeffler JA, Cawley LP, Moeder M. Serum IgE levels: correlation with skin test sensitivity. Ann Allergy 1973;31:331.
  6. Pepys J. Skin tests in diagnosis. In Gell PGH, Coombs RRA, Lachman PJ, eds. Clinical aspects of Immunology. Oxford: Blackwell Scientific Publications, 1975.
  7. Burrows B, et al. Respiratory disorders and allergy skin test reactions. Ann Allergy 1976;84:134.
  8. Implementation of Efficacy Review, Allergenic Extracts. Federal Register 1985;50:3082‑3288
  9. Levy DA, Lichenstein LM, Goldstein EO, Ishizaka K. Immunologic and cellular changes accompanying the therapy of pollen allergy. J Clin Invest 1973;50:360.
  10. Gurka G, Rocklin R. Immunologic responses during allergen-specific immunotherapy for respiratory allergy. Ann Allergy 1988;61:239-43.
  11. Zeiss CR Jr. Patient evaluation. In: Allergy and Clinical Immunology, Locky RF, ed. Garden City, N.Y.: Medical Examination Publishing 1976:616.
  12. Frankland AW, Augustin R. Prophylaxis of summer hay‑fever and asthma: a controlled trial comparing crude grass‑pollen extracts with the isolated main protein component. Lancet 1954;1:1055.
  13. Frankland AW, Augustin R. Grass pollen antigens effective in treatment. Clin Sci 1962;23:95.
  14. Rohr AS, Marshall NA, Saxon A: Successful immunotherapy for Triatoma protracta‑induced anaphylaxis. J Allergy Clin Immunol 1984;73:369‑75.
  15. Executive Committee, American Academy of Allergy and Immunology. The waiting period after allergen skin testing and immunotherapy (Position statement). J Allergy Clin Immunol 1990;85:526‑7.
  16. Greenberg MA, Kaufman CR, Gonzalez GE, Rosenblatt CD, Smith LJ, Summers RJ. Late and immediate systemic‑allergic reactions to inhalant allergen immunotherapy. J Allergy Clin Immunol 1986;77:865‑70.
  17. Ouellette JJ. Emergency management of the allergic reactions. Modern Medicine 1975;99.
  18. Anderson JA, et al. Personnel and equipment to treat systemic reactions caused by immunotherapy with allergenic extracts. J Allergy Clin Immunol 1986;77:271‑3.
  19. Sadan N, Rhyne MB, Mellits ED, et al. Immunotherapy of pollenosis in children: investigation of the immunologic basis of clinical improvement. N Eng J Med 1969;280:623.
  20. Johnstone DE. Value of hyposensitization therapy for perennial bronchial asthma in children. Pediatrics 1961;27:39.
  21. VanAsperin PP, Kemp AS, Mellis CM. Skin test reactivity and clinical allergen sensitivity in infancy. J Allergy Clin Immunol 1984;73:381‑6.
  22. Committee on Safety of Medicine. Desensitizing vaccines. Br Med J 1986;293:948.
  23. Lockey RF, Benedict LM, Turkeltaub PC, Bukantz SC. Fatalities from immunotherapy (IT) and skin testing (ST). J Allergy Clin Immunol 1987;79:660‑77.
  24. Norman PS, Van Metre TE Jr. The safety of allergenic immunotherapy. J Allergy Clin Immunol 1990;85:522‑5.

1600_Alternaria alternata_20000-pnu

1601_Alternaria alternata_40000-pnu1602_Alternaria alternata_20-wv1604_Alternaria alternata_1000-wv1605_Alternaria alternata_10000-pnu1606_Acremonium strictum_1000-wv1608_Aspergillus amsterdami_1000-wv1609_Aspergillus amsterdami_1000-pnu1610_Aspergillus flavus_20-wv1612_Aspergillus flavus_1000-wv1614_Aspergillus flavus_40000-pnu1615_Aspergillus fumigatus_10-wv1616_Aspergillus fumigatus_20000-pnu1617_Aspergillus fumigatus_40000-pnu1618_Aspergillus fumigatus_20-wv1619_Aspergillus fumigatus_500-wv1621_Aspergillus fumigatus_1000-wv1622_Aspergillus nidulans_10-wv1623_Aspergillus nidulans_1000-wv1625_Aspergillus niger_10-wv1626_Aspergillus niger_20-wv1627_Aspergillus niger_20000-pnu1628_Aspergillus niger_1000-wv1630_Aureobasidium pullulans_1000-wv1632_Bipolaris sorokiniana_10-wv1633_Bipolaris sorokiniana_40000-pnu1634_Bipolaris sorokiniana_20000-pnu1635_Bipolaris sorokiniana_20-wv1636_Bipolaris sorokiniana_1000-wv1639_Botrytis cinerea_1000-wv1640_Candida albicans_100-wv1641_Candida albicans_10-wv1642_Candida albicans_20000-pnu1643_Candida albicans_20-wv1644_Candida albicans_40000-pnu1646_Candida albicans_1000-wv1647_Chaetomium globosum_10-wv1648_Chaetomium globosum_40000-pnu1650_Chaetomium globosum_40000-pnu1651_Chaetomium globosum_1000-wv1653_Clado herbarum_20-wv1654_Clado herbarum_20000-pnu1656_Clado herbarum_1000-wv1657_Clado herbarum_40000-pnu1659_Clado sphaero_1000-wv1660_Drechslera spicifera_20-wv1661_Drechslera spicifera_40000-pnu1662_Drechslera spicifera_20000-pnu1664_Drechslera spicifera_1000-wv1666_Epicoccum nigrum_1000-wv1667_E floccosum_20-wv1668_E floccosum_1000-wv1669_E floccosum_1000-pnu1670_Fusarium moniliforme_10-wv1671_Fusarium moniliforme_20000-pnu1672_Fusarium moniliforme_20-wv1673_Fusarium moniliforme_40000-pnu1674_Fusarium moniliforme_1000-wv1676_Fusarium solani_40-wv1677_Fusarium solani_20000-pnu1678_Fusarium solani_1000-wv1680_Geotrichum candidum_1000-wv1681_Gliocladium viride_10-wv1682_Gliocladium viride_20-wv1683_Gliocladium viride_1000-wv1684_Gliocladium viride_1000-pnu1685_Gliocladium viride_20000-pnu1686_Gliocladium viride_40000-pnu1687_Helminthosporium solani_1000-wv1689_Helminthosporium solani_10-wv1690_Helminthosporium solani_20-wv1691_Helminthosporium solani_40000-pnu1692_Mucor cir f circinelloides_20000-pnu1694_Mucor plumbeus_10-wv1695_Mucor plumbeus_20000-pnu1696_Mucor plumbeus_40000-pnu1698_Mucor plumbeus_1000-wv1699_Neurospora intermedia_10-wv2600_Neurospora intermedia_40000-pnu2601_Neurospora intermedia_20000-pnu2602_Neurospora intermedia_1000-wv2605_Paecilomyces varioti_10-wv2606_Paecilomyces varioti_20000-pnu2607_Paecilomyces varioti_1000-pnu2608_Paecilomyces varioti_1000-wv2609_Paecilomyces varioti_40000-pnu2610_Penicillium digitatum_40-wv2612_Penicillium chrysogenum (notatum)_1000-wv2614_Penicillium chrysogenum (notatum)_10-wv2615_Penicillium chrysogenum (notatum)_40000-pnu2616_Penicillium chrysogenum (notatum)_20000-pnu2618_Phoma betae_1000-wv2619_Rhizopus oryzae_10-wv2620_Rhizopus oryzae_20000-pnu2621_Rhizopus oryzae_1000-wv2623_Rhizopus stolonifer_20-wv2624_Rhizopus stolonifer_40000-pnu2625_Rhizopus stolonifer_200002627_Rhizopus stolonifer_1000-wv2628_Rhodotorula mucilaginosa_1000-wv2630_Rhodotorula mucilaginosa_20-wv2631_Rhodotorula mucilaginosa_40000-pnu2633_Saccharomyces cerevisiae_1000-wv2634_Saccharomyces cerevisiae_10-wv2635_Stemphylium solani_20-wv2636_Stemphylium solani_20000-pnu2637_Stemphylium solani_40000-pnu2638_Stemphylium solani_1000-wv2640_Trichoderma harzianum_20-wv2641_Trichoderma harzianum_40000-pnu2642_Trichoderma harzianum_1000-wv2644_Trichophyton mentagrophytes_10-wv2645_Trichophyton mentagrophytes_20000-pnu2646_Trichophyton mentagrophytes_20-wv2648_Trichophyton mentagrophytes_1000-wv2649_Trichophyton mentagrophytes_40000-pnu2650_Trichophyton rubrum_1000-wv2652_Trichithecium roseum_10-wv2653_Trichithecium roseum_40000-pnu2654_Trichithecium roseum_20000-pnu2655_Trichithecium roseum_1000-wv2656_Trichithecium roseum_1000-pnu2659_Mucor cir f lusitanicus_1000-wv2660_Aspergillus nidulans_20000-pnu2661_Bipolaris sorokiniana_10000-pnu2662_Botrytis cinerea_20-wv2663_Clado sphaero_10-wv2664_Ustilago maydis_10-wv2665_Epicoccum nigrum_20-wv2666_E floccosum_10-wv2667_Geotrichum candidum_10-wv2668_Helminthosporium solani_20000-pnu2669_Mucor cir f circinelloides_10-wv2670_Mucor cir f circinelloides_20-wv2671_Mucor cir f lusitanicus_10-wv2672_Mucor plumbeus_20-wv2673_Paecilomyces varioti_20-wv2674_Phoma betae_20-wv2675_Rhodotorula mucilaginosa_20000-pnu2676_Saccharomyces cerevisiae_20000-pnu2677_Saccharomyces cerevisiae_20-wv2678_Saccharomyces cerevisiae_40000-pnu2679_Acremonium strictum_10-wv2680_Trichoderma harzianum_20000-PNU2681_Trichophyton rubrum_10-wv5600_Alternaria alternata_20-wv5601_Acremonium strictum_20-wv5602_Aspergillus amsterdami_20-wv5603_Aspergillus flavus_40-wv5604_Aspergillus fumigatus_20-wv5605_Aspergillus nidulans_20wv5606_Aspergillus niger_20-wv5607_Aureobasidium pullulans_40-wv5608_Bipolaris sorokiniana_20-wv5609_Botrytis cinerea_40-wv5610_Candida albicans_20-wv5612_Chaetomium globosum_20-wv5613_Cladosporium herbarum_40-wv5614_Cladosporium sphaerospermum_20-wv5615_Drechslera spicifera_40-wv5616_Epicoccum nigrum_40-wv5617_Epidermophyton floccosum_20-wv5618_Fusarium moniliforme_20-wv5619_Fusarium solani_40-wv5620_Geotrichum candidum_20-wv5621_Gliocladium viride_20-wv5622_Helminthosporium solani_20-wv5623_Microsporum canis_20-wv5624_Mucor cir f. circinelloides_20-wv5625_Mucor cir f. lusitanicus_20-wv
5626_Mucor plumbeus_20-wv
(click image for full-size original)
5627_Neurospora intermedia_20-wv5629_Paecilomyces varioti_20-wv5630_Penicillium digitatum_80-wv5631_Penicillium chrysogenum (notatum)_20-wv5632_Phoma betae_40-wv5633_Rhizopus oryzae_20-wv5634_Rhizopus stolonifer_40-wv5635_Rhodotorula mucilaginosa_40-wv5636_Saccharomyces cerevisiae_20-wv5637_Stemphylium solani_40-wv5638_Trichoderma harzianum_40-wv5639_Trichophyton mentagrophytes_20-wv5640_Trichophyton rubrum_20-wv5641_Trichothecium roseum_20-wv5642_Mycogone perniciosa_20-wv5648_Ustilago cynodontis_20-wv9600_Mold Mix 1_10-wv9601_Mold Mix 1_20000-pnu9602_Mold Mix 1_40000-pnu9603_Mold Mix 1_20-wv9604_Mold Mix 1_1000-wv9606_Mold Mix 1_20-wv9607_Mold Mix 2_20-wv9608_Mold Mix 2_20000-pnu9609_Mold Mix 2_10000-pnu9610_Mold Mix 2_40000-pnu9612_Mold Mix 2_1000-wv9613_Mold Mix 2_40-wv9614_GS Mold Mix 3_1000-wv9616_Mold Mix 3_20000-pnu9617_Mold Mix 3_10-wv9618_Mold Mix 3_40000-pnu9619_Mold Mix 3_20-wv9620_Mold Mix 3_20-wv9621_AHH Mold Mix_20-wv9622_AHH Mold Mix_1000-wv9623_AHH Mold Mix_20-wv9624_Alternaria_Hormodendrum Mix_20-wv9625_Alternaria_Hormodendrum Mix_1000-wv9626_Alternaria_Hormodendrum Mix_20-wv9627_Aspergillus Mix_10-wv9628_Aspergillus Mix_40000-pnu9629_Aspergillus Mix_20000-pnu9630_Aspergillus Mix_20-wv9631_Aspergillus Mix_1000-wv9633_Aspergillus Mix_20-wv9634_Dematiaceae Mix_20-wv9635_Dematiaceae Mix_40-wv9636_Fusarium Mix_20-wv9637_Fusarium Mix_40000-pnu9638_Fusarium Mix_20000-pnu9639_Fusarium Mix_1000-wv9641_Fusarium Mix_40-wv9642_Monilia Mix_20000-pnu9643_Monilia Mix_1000-pnu9644_Monilia Mix_1000-wv9645_Monilia Mix_20-wv9646_Mucor Mix_1000-wv9648_Mucor Mix_20-wv9649_New Stock Fungi Mix_10-wv9650_New Stock Fungi Mix_1000-wv9651_New Stock Fungi Mix_20000-pnu9652_New Stock Fungi Mix_20-wv9653_New Stock Fungi Mix_20-wv9654_Penicillium Mix_10-wv9655_Penicillium Mix_40000-pnu9656_Penicillium Mix_20000-pnu9657_Penicillium Mix_20-wv9659_Penicillium Mix_1000-wv9660_Penicillium Mix_20-wv9661_Phycomycetes Mix_20-wv9662_Phycomycetes Mix_1000-wv9664_Phycomycetes Mix_40-wv9665_Rhizopus Mix_20-wv9666_Rhizopus Mix_40000-pnu9668_Rhizopus Mix_1000-wv9669_Rhizopus Mix_40-wv
9670_Grain Smut Mix_40-wv
(click image for full-size original)
9671_Grass Smut Mix_20-wv9672_Mucor Mix_10-wv9673_AHH Mold Mix_40000-pnu9674_Alternaria_Hormodendrum Mix_20000-pnu9675_Grain Smut Mix_20-wv9676_Grass Smut Mix_10-wv9677_Monilia Mix_10-wv9678_New Stock Fungi Mix_40000-pnu9679_Penicillium Mix_10000-pnu9680_Rhizopus Mix_20000-pnu1600_Alternaria alternata_20000-pnu1601_Alternaria alternata_40000-pnu1602_Alternaria alternata_20-wv1604_Alternaria alternata_1000-wv1605_Alternaria alternata_10000-pnu1606_Acremonium strictum_1000-wv1608_Aspergillus amsterdami_1000-wv1609_Aspergillus amsterdami_1000-pnu1610_Aspergillus flavus_20-wv1612_Aspergillus flavus_1000-wv1614_Aspergillus flavus_40000-pnu1615_Aspergillus fumigatus_10-wv1616_Aspergillus fumigatus_20000-pnu1617_Aspergillus fumigatus_40000-pnu1618_Aspergillus fumigatus_20-wv1619_Aspergillus fumigatus_500-wv1621_Aspergillus fumigatus_1000-wv1622_Aspergillus nidulans_10-wv1623_Aspergillus nidulans_1000-wv1625_Aspergillus niger_10-wv1626_Aspergillus niger_20-wv1627_Aspergillus niger_20000-pnu1628_Aspergillus niger_1000-wv1630_Aureobasidium pullulans_1000-wv1632_Bipolaris sorokiniana_10-wv1633_Bipolaris sorokiniana_40000-pnu1634_Bipolaris sorokiniana_20000-pnu1635_Bipolaris sorokiniana_20-wv1636_Bipolaris sorokiniana_1000-wv1639_Botrytis cinerea_1000-wv1640_Candida albicans_100-wv1641_Candida albicans_10-wv1642_Candida albicans_20000-pnu1643_Candida albicans_20-wv1644_Candida albicans_40000-pnu1646_Candida albicans_1000-wv1647_Chaetomium globosum_10-wv1648_Chaetomium globosum_40000-pnu1650_Chaetomium globosum_40000-pnu1651_Chaetomium globosum_1000-wv1653_Clado herbarum_20-wv1654_Clado herbarum_20000-pnu1656_Clado herbarum_1000-wv1657_Clado herbarum_40000-pnu1659_Clado sphaero_1000-wv1660_Drechslera spicifera_20-wv1661_Drechslera spicifera_40000-pnu1662_Drechslera spicifera_20000-pnu1664_Drechslera spicifera_1000-wv1666_Epicoccum nigrum_1000-wv1667_E floccosum_20-wv1668_E floccosum_1000-wv1669_E floccosum_1000-pnu1670_Fusarium moniliforme_10-wv1671_Fusarium moniliforme_20000-pnu1672_Fusarium moniliforme_20-wv1673_Fusarium moniliforme_40000-pnu1674_Fusarium moniliforme_1000-wv1676_Fusarium solani_40-wv1677_Fusarium solani_20000-pnu1678_Fusarium solani_1000-wv1680_Geotrichum candidum_1000-wv1681_Gliocladium viride_10-wv1682_Gliocladium viride_20-wv1683_Gliocladium viride_1000-wv1684_Gliocladium viride_1000-pnu1685_Gliocladium viride_20000-pnu1686_Gliocladium viride_40000-pnu1687_Helminthosporium solani_1000-wv1689_Helminthosporium solani_10-wv1690_Helminthosporium solani_20-wv1691_Helminthosporium solani_40000-pnu1692_Mucor cir f circinelloides_20000-pnu1694_Mucor plumbeus_10-wv1695_Mucor plumbeus_20000-pnu1696_Mucor plumbeus_40000-pnu1698_Mucor plumbeus_1000-wv1699_Neurospora intermedia_10-wv2600_Neurospora intermedia_40000-pnu2601_Neurospora intermedia_20000-pnu2602_Neurospora intermedia_1000-wv2605_Paecilomyces varioti_10-wv2606_Paecilomyces varioti_20000-pnu2607_Paecilomyces varioti_1000-pnu2608_Paecilomyces varioti_1000-wv2609_Paecilomyces varioti_40000-pnu2610_Penicillium digitatum_40-wv2612_Penicillium chrysogenum (notatum)_1000-wv2614_Penicillium chrysogenum (notatum)_10-wv2615_Penicillium chrysogenum (notatum)_40000-pnu2616_Penicillium chrysogenum (notatum)_20000-pnu2618_Phoma betae_1000-wv2619_Rhizopus oryzae_10-wv2620_Rhizopus oryzae_20000-pnu2621_Rhizopus oryzae_1000-wv2623_Rhizopus stolonifer_20-wv2624_Rhizopus stolonifer_40000-pnu2625_Rhizopus stolonifer_200002627_Rhizopus stolonifer_1000-wv2628_Rhodotorula mucilaginosa_1000-wv2630_Rhodotorula mucilaginosa_20-wv2631_Rhodotorula mucilaginosa_40000-pnu2633_Saccharomyces cerevisiae_1000-wv2634_Saccharomyces cerevisiae_10-wv2635_Stemphylium solani_20-wv2636_Stemphylium solani_20000-pnu2637_Stemphylium solani_40000-pnu2638_Stemphylium solani_1000-wv2640_Trichoderma harzianum_20-wv2641_Trichoderma harzianum_40000-pnu2642_Trichoderma harzianum_1000-wv2644_Trichophyton mentagrophytes_10-wv2645_Trichophyton mentagrophytes_20000-pnu2646_Trichophyton mentagrophytes_20-wv2648_Trichophyton mentagrophytes_1000-wv2649_Trichophyton mentagrophytes_40000-pnu2650_Trichophyton rubrum_1000-wv2652_Trichithecium roseum_10-wv2653_Trichithecium roseum_40000-pnu2654_Trichithecium roseum_20000-pnu2655_Trichithecium roseum_1000-wv2656_Trichithecium roseum_1000-pnu2659_Mucor cir f lusitanicus_1000-wv2660_Aspergillus nidulans_20000-pnu2661_Bipolaris sorokiniana_10000-pnu2662_Botrytis cinerea_20-wv2663_Clado sphaero_10-wv2664_Ustilago maydis_10-wv2665_Epicoccum nigrum_20-wv2666_E floccosum_10-wv2667_Geotrichum candidum_10-wv2668_Helminthosporium solani_20000-pnu2669_Mucor cir f circinelloides_10-wv2670_Mucor cir f circinelloides_20-wv2671_Mucor cir f lusitanicus_10-wv2672_Mucor plumbeus_20-wv2673_Paecilomyces varioti_20-wv2674_Phoma betae_20-wv2675_Rhodotorula mucilaginosa_20000-pnu2676_Saccharomyces cerevisiae_20000-pnu2677_Saccharomyces cerevisiae_20-wv2678_Saccharomyces cerevisiae_40000-pnu2679_Acremonium strictum_10-wv2680_Trichoderma harzianum_20000-PNU2681_Trichophyton rubrum_10-wv5600_Alternaria alternata_20-wv5601_Acremonium strictum_20-wv5602_Aspergillus amsterdami_20-wv5603_Aspergillus flavus_40-wv5604_Aspergillus fumigatus_20-wv5605_Aspergillus nidulans_20wv5606_Aspergillus niger_20-wv5607_Aureobasidium pullulans_40-wv5608_Bipolaris sorokiniana_20-wv5609_Botrytis cinerea_40-wv5610_Candida albicans_20-wv5612_Chaetomium globosum_20-wv5613_Cladosporium herbarum_40-wv5614_Cladosporium sphaerospermum_20-wv5615_Drechslera spicifera_40-wv5616_Epicoccum nigrum_40-wv5617_Epidermophyton floccosum_20-wv5618_Fusarium moniliforme_20-wv5619_Fusarium solani_40-wv5620_Geotrichum candidum_20-wv5621_Gliocladium viride_20-wv5622_Helminthosporium solani_20-wv5623_Microsporum canis_20-wv5624_Mucor cir f. circinelloides_20-wv5625_Mucor cir f. lusitanicus_20-wv5626_Mucor plumbeus_20-wv5627_Neurospora intermedia_20-wv5629_Paecilomyces varioti_20-wv5630_Penicillium digitatum_80-wv5631_Penicillium chrysogenum (notatum)_20-wv5632_Phoma betae_40-wv5633_Rhizopus oryzae_20-wv5634_Rhizopus stolonifer_40-wv5635_Rhodotorula mucilaginosa_40-wv5636_Saccharomyces cerevisiae_20-wv5637_Stemphylium solani_40-wv5638_Trichoderma harzianum_40-wv5639_Trichophyton mentagrophytes_20-wv5640_Trichophyton rubrum_20-wv5641_Trichothecium roseum_20-wv5642_Mycogone perniciosa_20-wv5648_Ustilago cynodontis_20-wv9600_Mold Mix 1_10-wv9601_Mold Mix 1_20000-pnu9602_Mold Mix 1_40000-pnu9603_Mold Mix 1_20-wv9604_Mold Mix 1_1000-wv9606_Mold Mix 1_20-wv9607_Mold Mix 2_20-wv9608_Mold Mix 2_20000-pnu9609_Mold Mix 2_10000-pnu9610_Mold Mix 2_40000-pnu9612_Mold Mix 2_1000-wv9613_Mold Mix 2_40-wv9614_GS Mold Mix 3_1000-wv9616_Mold Mix 3_20000-pnu9617_Mold Mix 3_10-wv9618_Mold Mix 3_40000-pnu9619_Mold Mix 3_20-wv9620_Mold Mix 3_20-wv9621_AHH Mold Mix_20-wv9622_AHH Mold Mix_1000-wv9623_AHH Mold Mix_20-wv9624_Alternaria_Hormodendrum Mix_20-wv9625_Alternaria_Hormodendrum Mix_1000-wv9626_Alternaria_Hormodendrum Mix_20-wv9627_Aspergillus Mix_10-wv9628_Aspergillus Mix_40000-pnu9629_Aspergillus Mix_20000-pnu9630_Aspergillus Mix_20-wv9631_Aspergillus Mix_1000-wv9633_Aspergillus Mix_20-wv9634_Dematiaceae Mix_20-wv9635_Dematiaceae Mix_40-wv9636_Fusarium Mix_20-wv9637_Fusarium Mix_40000-pnu9638_Fusarium Mix_20000-pnu9639_Fusarium Mix_1000-wv9641_Fusarium Mix_40-wv9642_Monilia Mix_20000-pnu9643_Monilia Mix_1000-pnu9644_Monilia Mix_1000-wv9645_Monilia Mix_20-wv9646_Mucor Mix_1000-wv9648_Mucor Mix_20-wv9649_New Stock Fungi Mix_10-wv9650_New Stock Fungi Mix_1000-wv9651_New Stock Fungi Mix_20000-pnu9652_New Stock Fungi Mix_20-wv9653_New Stock Fungi Mix_20-wv9654_Penicillium Mix_10-wv9655_Penicillium Mix_40000-pnu9656_Penicillium Mix_20000-pnu9657_Penicillium Mix_20-wv9659_Penicillium Mix_1000-wv9660_Penicillium Mix_20-wv9661_Phycomycetes Mix_20-wv9662_Phycomycetes Mix_1000-wv9664_Phycomycetes Mix_40-wv9665_Rhizopus Mix_20-wv9666_Rhizopus Mix_40000-pnu9668_Rhizopus Mix_1000-wv9669_Rhizopus Mix_40-wv9670_Grain Smut Mix_40-wv9671_Grass Smut Mix_20-wv9672_Mucor Mix_10-wv9673_AHH Mold Mix_40000-pnu9674_Alternaria_Hormodendrum Mix_20000-pnu9675_Grain Smut Mix_20-wv9676_Grass Smut Mix_10-wv9677_Monilia Mix_10-wv9678_New Stock Fungi Mix_40000-pnu9679_Penicillium Mix_10000-pnu9680_Rhizopus Mix_20000-pnu
PENICILLIUM MIX penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9660
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM DIGITATUM (PENICILLIUM DIGITATUM) PENICILLIUM DIGITATUM 0.0125 g in 1 mL
PENICILLIUM CAMEMBERTI (PENICILLIUM CAMEMBERTI) PENICILLIUM CAMEMBERTI 0.0125 g in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.0125 g in 1 mL
PENICILLIUM ROQUEFORTI (PENICILLIUM ROQUEFORTI) PENICILLIUM ROQUEFORTI 0.0125 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9660-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9660-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-9660-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981 10/01/2019
PENICILLIUM MIX penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9659
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM CAMEMBERTI (PENICILLIUM CAMEMBERTI) PENICILLIUM CAMEMBERTI 0.00025 g in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.00025 g in 1 mL
PENICILLIUM ROQUEFORTI (PENICILLIUM ROQUEFORTI) PENICILLIUM ROQUEFORTI 0.00025 g in 1 mL
PENICILLIUM DIGITATUM (PENICILLIUM DIGITATUM) PENICILLIUM DIGITATUM 0.00025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9659-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981 10/01/2019
PHYCOMYCETES MIX mucor circinelloides f. lusitanicus and rhizopus stolonifer solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9661
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (MUCOR CIRCINELLOIDES F. LUSITANICUS) MUCOR CIRCINELLOIDES F. LUSITANICUS 0.025 g in 1 mL
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9661-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PHYCOMYCETES MIX mucor circinelloides f. lusitanicus and rhizopus stolonifer solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9662
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (MUCOR CIRCINELLOIDES F. LUSITANICUS) MUCOR CIRCINELLOIDES F. LUSITANICUS 0.0005 g in 1 mL
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.0005 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9662-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PHYCOMYCETES MIX mucor circinelloides f. lusitanicus and rhizopus stolonifer solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9664
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (MUCOR CIRCINELLOIDES F. LUSITANICUS) MUCOR CIRCINELLOIDES F. LUSITANICUS 0.0125 g in 1 mL
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.0125 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9664-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9664-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-9664-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHIZOPUS MIX rhizopus stolonifer and rhizopus oryzae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9665
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.025 g in 1 mL
RHIZOPUS ARRHIZUS (RHIZOPUS ARRHIZUS) RHIZOPUS ARRHIZUS 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9665-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9665-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHIZOPUS MIX rhizopus stolonifer and rhizopus oryzae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9666
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 20000 [PNU] in 1 mL
RHIZOPUS ARRHIZUS (RHIZOPUS ARRHIZUS) RHIZOPUS ARRHIZUS 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9666-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHIZOPUS MIX rhizopus stolonifer and rhizopus oryzae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9668
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.0005 g in 1 mL
RHIZOPUS ARRHIZUS (RHIZOPUS ARRHIZUS) RHIZOPUS ARRHIZUS 0.0005 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9668-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS FLAVUS aspergillus flavus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1612
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FLAVUS (ASPERGILLUS FLAVUS) ASPERGILLUS FLAVUS 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1612-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
BIPOLARIS SOROKINIANA bipolaris sorokiniana solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2661
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2661-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PENICILLIUM DIGITATUM penicillium digitatum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2610
Route of Administration INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM DIGITATUM (PENICILLIUM DIGITATUM) PENICILLIUM DIGITATUM 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2610-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2610-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR MIX mucor circinelloides f. lusitanicus and mucor plumbeus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9672
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (MUCOR CIRCINELLOIDES F. LUSITANICUS) MUCOR CIRCINELLOIDES F. LUSITANICUS 0.05 g in 1 mL
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9672-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 2 aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9607
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.01 g in 1 mL
COCHLIOBOLUS SPICIFER (COCHLIOBOLUS SPICIFER) COCHLIOBOLUS SPICIFER 0.01 g in 1 mL
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.01 g in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.01 g in 1 mL
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.01 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9607-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9607-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS MIX aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9628
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 8000 [PNU] in 1 mL
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 8000 [PNU] in 1 mL
EUROTIUM AMSTELODAMI (EUROTIUM AMSTELODAMI) EUROTIUM AMSTELODAMI 8000 [PNU] in 1 mL
ASPERGILLUS FLAVUS (ASPERGILLUS FLAVUS) ASPERGILLUS FLAVUS 8000 [PNU] in 1 mL
ASPERGILLUS NIDULANS (ASPERGILLUS NIDULANS) ASPERGILLUS NIDULANS 8000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9628-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9628-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS MIX aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9633
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.01 g in 1 mL
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 0.01 g in 1 mL
EUROTIUM AMSTELODAMI (EUROTIUM AMSTELODAMI) EUROTIUM AMSTELODAMI 0.01 g in 1 mL
ASPERGILLUS FLAVUS (ASPERGILLUS FLAVUS) ASPERGILLUS FLAVUS 0.01 g in 1 mL
ASPERGILLUS NIDULANS (ASPERGILLUS NIDULANS) ASPERGILLUS NIDULANS 0.01 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9633-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9633-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-9633-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MONILIA MIX candida albicans and neurospora intermedia solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9644
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 0.0005 g in 1 mL
NEUROSPORA INTERMEDIA (NEUROSPORA INTERMEDIA) NEUROSPORA INTERMEDIA 0.0005 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9644-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS FUMIGATUS aspergillus fumigatus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1616
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1616-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS FLAVUS aspergillus flavus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1614
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FLAVUS (ASPERGILLUS FLAVUS) ASPERGILLUS FLAVUS 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1614-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS FUMIGATUS aspergillus fumigatus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5604
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5604-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5604-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5604-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
AUREOBASIDIUM PULLULANS aureobasidium pullulans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5607
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5607-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5607-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5607-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 3 alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9620
Route of Administration INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.0125 g in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.0125 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.0125 g in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.0125 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9620-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9620-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-9620-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 2 aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9613
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.005 g in 1 mL
COCHLIOBOLUS SPICIFER (COCHLIOBOLUS SPICIFER) COCHLIOBOLUS SPICIFER 0.005 g in 1 mL
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.005 g in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.005 g in 1 mL
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.005 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9613-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9613-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-9613-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
DRECHSLERA SPICIFERA drechslera spicifera solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1660
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SPICIFER (COCHLIOBOLUS SPICIFER) COCHLIOBOLUS SPICIFER 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1660-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1660-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
EPIDERMOPHYTON FLOCCOSUM epidermophyton floccosum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2666
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EPIDERMOPHYTON FLOCCOSUM (EPIDERMOPHYTON FLOCCOSUM) EPIDERMOPHYTON FLOCCOSUM 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2666-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES mucor circinelloides f. circinelloides solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1692
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (MUCOR CIRCINELLOIDES F. CIRCINELLOIDES) MUCOR CIRCINELLOIDES F. CIRCINELLOIDES 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1692-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES mucor circinelloides f. circinelloides solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2670
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (MUCOR CIRCINELLOIDES F. CIRCINELLOIDES) MUCOR CIRCINELLOIDES F. CIRCINELLOIDES 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2670-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
NEUROSPORA INTERMEDIA neurospora intermedia solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1699
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NEUROSPORA INTERMEDIA (NEUROSPORA INTERMEDIA) NEUROSPORA INTERMEDIA 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1699-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1699-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
NEUROSPORA INTERMEDIA neurospora intermedia solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2602
Route of Administration SUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NEUROSPORA INTERMEDIA (NEUROSPORA INTERMEDIA) NEUROSPORA INTERMEDIA 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2602-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PAECILOMYCES VARIOTII paecilomyces variotii solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2673
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PAECILOMYCES VARIOTII (PAECILOMYCES VARIOTII) PAECILOMYCES VARIOTII 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2673-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PENICILLIUM CHRYSOGENUM (NOTATUM) penicillium chrysogenum (notatum) solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2616
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2616-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PHOMA BETAE phoma betae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2618
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PLEOSPORA BETAE (PLEOSPORA BETAE) PLEOSPORA BETAE 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2618-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM MONILIFORME fusarium moniliforme solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1672
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1672-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
GEOTRICHUM CANDIDUM geotrichum candidum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5620
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GEOTRICHUM CANDIDUM (GEOTRICHUM CANDIDUM) GEOTRICHUM CANDIDUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5620-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5620-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5620-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PENICILLIUM CHRYSOGENUM (NOTATUM) penicillium chrysogenum (notatum) solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2612
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2612-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHIZOPUS ORYZAE rhizopus oryzae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2621
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS ARRHIZUS (RHIZOPUS ARRHIZUS) RHIZOPUS ARRHIZUS 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2621-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHODOTORULA MUCILAGINOSA rhodotorula mucilaginosa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2630
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHODOTORULA MUCILAGINOSA (RHODOTORULA MUCILAGINOSA) RHODOTORULA MUCILAGINOSA 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2630-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2630-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
SACCHAROMYCES CEREVISIAE saccharomyces cerevisiae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2633
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SACCHAROMYCES CEREVISIAE (SACCHAROMYCES CEREVISIAE) SACCHAROMYCES CEREVISIAE 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2633-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ALTERNARIA ALTERNATA alternaria alternata solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1602
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1602-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1602-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM MONILIFORME fusarium moniliforme solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5618
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5618-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5618-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5618-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
GEOTRICHUM CANDIDUM geotrichum candidum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2667
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GEOTRICHUM CANDIDUM (GEOTRICHUM CANDIDUM) GEOTRICHUM CANDIDUM 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2667-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
GLIOCLADIUM VIRIDE gliocladium viride solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1685
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GLIOCLADIUM VIRIDE (GLIOCLADIUM VIRIDE) GLIOCLADIUM VIRIDE 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1685-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1685-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
GLIOCLADIUM VIRIDE gliocladium viride solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1686
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GLIOCLADIUM VIRIDE (GLIOCLADIUM VIRIDE) GLIOCLADIUM VIRIDE 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1686-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
HELMINTHOSPORIUM SOLANI helminthosporium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1689
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HELMINTHOSPORIUM SOLANI (HELMINTHOSPORIUM SOLANI) HELMINTHOSPORIUM SOLANI 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1689-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1689-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR PLUMBEUS mucor plumbeus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1695
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1695-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR PLUMBEUS mucor plumbeus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2672
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2672-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PAECILOMYCES VARIOTII paecilomyces variotii solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2608
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PAECILOMYCES VARIOTII (PAECILOMYCES VARIOTII) PAECILOMYCES VARIOTII 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2608-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHIZOPUS ORYZAE rhizopus oryzae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2620
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS ARRHIZUS (RHIZOPUS ARRHIZUS) RHIZOPUS ARRHIZUS 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2620-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
HELMINTHOSPORIUM SOLANI helminthosporium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1687
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HELMINTHOSPORIUM SOLANI (HELMINTHOSPORIUM SOLANI) HELMINTHOSPORIUM SOLANI 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1687-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHODOTORULA MUCILAGINOSA rhodotorula mucilaginosa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2631
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHODOTORULA MUCILAGINOSA (RHODOTORULA MUCILAGINOSA) RHODOTORULA MUCILAGINOSA 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2631-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHODOTORULA MUCILAGINOSA rhodotorula mucilaginosa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2675
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHODOTORULA MUCILAGINOSA (RHODOTORULA MUCILAGINOSA) RHODOTORULA MUCILAGINOSA 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2675-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHODOTORULA MUCILAGINOSA rhodotorula mucilaginosa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5635
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHODOTORULA MUCILAGINOSA (RHODOTORULA MUCILAGINOSA) RHODOTORULA MUCILAGINOSA 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5635-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5635-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5635-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHODERMA HARZIANUM trichoderma harzianum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2641
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHODERMA HARZIANUM (TRICHODERMA HARZIANUM) TRICHODERMA HARZIANUM 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2641-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2641-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHODERMA HARZIANUM trichoderma harzianum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2680
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHODERMA HARZIANUM (TRICHODERMA HARZIANUM) TRICHODERMA HARZIANUM 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2680-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOPHYTON MENTAGROPHYTES trichophyton mentagrophytes solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2644
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOPHYTON MENTAGROPHYTES (TRICHOPHYTON MENTAGROPHYTES) TRICHOPHYTON MENTAGROPHYTES 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2644-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOPHYTON MENTAGROPHYTES trichophyton mentagrophytes solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2648
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOPHYTON MENTAGROPHYTES (TRICHOPHYTON MENTAGROPHYTES) TRICHOPHYTON MENTAGROPHYTES 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2648-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOPHYTON MENTAGROPHYTES trichophyton mentagrophytes solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5639
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOPHYTON MENTAGROPHYTES (TRICHOPHYTON MENTAGROPHYTES) TRICHOPHYTON MENTAGROPHYTES 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5639-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5639-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOPHYTON RUBRUM trichophyton rubrum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2650
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOPHYTON RUBRUM (TRICHOPHYTON RUBRUM) TRICHOPHYTON RUBRUM 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2650-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOPHYTON RUBRUM trichophyton rubrum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2681
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOPHYTON RUBRUM (TRICHOPHYTON RUBRUM) TRICHOPHYTON RUBRUM 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2681-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOTHECIUM ROSEUM trichothecium roseum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2652
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOTHECIUM ROSEUM (TRICHOTHECIUM ROSEUM) TRICHOTHECIUM ROSEUM 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2652-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2652-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOTHECIUM ROSEUM trichothecium roseum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2653
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOTHECIUM ROSEUM (TRICHOTHECIUM ROSEUM) TRICHOTHECIUM ROSEUM 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2653-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2653-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOTHECIUM ROSEUM trichothecium roseum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2655
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOTHECIUM ROSEUM (TRICHOTHECIUM ROSEUM) TRICHOTHECIUM ROSEUM 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2655-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOTHECIUM ROSEUM trichothecium roseum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5641
Route of Administration SUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOTHECIUM ROSEUM (TRICHOTHECIUM ROSEUM) TRICHOTHECIUM ROSEUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5641-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5641-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5641-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ALTERNARIA ALTERNATA alternaria alternata solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5600
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5600-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5600-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
SACCHAROMYCES CEREVISIAE saccharomyces cerevisiae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2676
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SACCHAROMYCES CEREVISIAE (SACCHAROMYCES CEREVISIAE) SACCHAROMYCES CEREVISIAE 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2676-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
SACCHAROMYCES CEREVISIAE saccharomyces cerevisiae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2678
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SACCHAROMYCES CEREVISIAE (SACCHAROMYCES CEREVISIAE) SACCHAROMYCES CEREVISIAE 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2678-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
SACCHAROMYCES CEREVISIAE saccharomyces cerevisiae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5636
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SACCHAROMYCES CEREVISIAE (SACCHAROMYCES CEREVISIAE) SACCHAROMYCES CEREVISIAE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5636-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5636-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
STEMPHYLIUM SOLANI stemphylium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2635
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
STEMPHYLIUM SOLANI (STEMPHYLIUM SOLANI) STEMPHYLIUM SOLANI 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2635-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2635-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
STEMPHYLIUM SOLANI stemphylium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2638
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
STEMPHYLIUM SOLANI (STEMPHYLIUM SOLANI) STEMPHYLIUM SOLANI 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2638-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOPHYTON MENTAGROPHYTES trichophyton mentagrophytes solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2649
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOPHYTON MENTAGROPHYTES (TRICHOPHYTON MENTAGROPHYTES) TRICHOPHYTON MENTAGROPHYTES 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2649-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR CIRCINELLOIDES F. LUSITANICUS mucor circinelloides f. lusitanicus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2659
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (MUCOR CIRCINELLOIDES F. LUSITANICUS) MUCOR CIRCINELLOIDES F. LUSITANICUS 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2659-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
EPICOCCUM NIGRUM epicoccum nigrum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5616
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EPICOCCUM NIGRUM (EPICOCCUM NIGRUM) EPICOCCUM NIGRUM 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5616-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5616-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
EPIDERMOPHYTON FLOCCOSUM epidermophyton floccosum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5617
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EPIDERMOPHYTON FLOCCOSUM (EPIDERMOPHYTON FLOCCOSUM) EPIDERMOPHYTON FLOCCOSUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5617-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5617-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5617-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MICROSPORUM CANIS microsporum canis solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5623
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MICROSPORUM CANIS (MICROSPORUM CANIS) MICROSPORUM CANIS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5623-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5623-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5623-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
BERMUDA GRASS SMUT ustilago cynodontis solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5648
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
USTILAGO CYNODONTIS (USTILAGO CYNODONTIS) USTILAGO CYNODONTIS 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5648-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5648-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5648-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM MONILIFORME fusarium moniliforme solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1671
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1671-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1671-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS AMSTELODAMI aspergillus amstelodami solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1608
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EUROTIUM AMSTELODAMI (EUROTIUM AMSTELODAMI) EUROTIUM AMSTELODAMI 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1608-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS NIDULANS aspergillus nidulans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5605
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIDULANS (ASPERGILLUS NIDULANS) ASPERGILLUS NIDULANS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5605-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS NIGER aspergillus niger solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1626
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1626-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
BOTRYTIS CINEREA botrytis cinerea solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2662
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BOTRYTIS CINEREA (BOTRYTIS CINEREA) BOTRYTIS CINEREA 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2662-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CLADOSPORIUM HERBARUM cladosporium herbarum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1653
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM HERBARUM (CLADOSPORIUM HERBARUM) CLADOSPORIUM HERBARUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1653-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1653-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CLADOSPORIUM HERBARUM cladosporium herbarum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1654
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM HERBARUM (CLADOSPORIUM HERBARUM) CLADOSPORIUM HERBARUM 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1654-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1654-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CLADOSPORIUM HERBARUM cladosporium herbarum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1656
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM HERBARUM (CLADOSPORIUM HERBARUM) CLADOSPORIUM HERBARUM 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1656-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ALTERNARIA ALTERNATA alternaria alternata solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1605
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1605-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS AMSTELODAMI aspergillus amstelodami solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1609
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EUROTIUM AMSTELODAMI (EUROTIUM AMSTELODAMI) EUROTIUM AMSTELODAMI 1000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1609-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
BOTRYTIS CINEREA botrytis cinerea solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1639
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BOTRYTIS CINEREA (BOTRYTIS CINEREA) BOTRYTIS CINEREA 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1639-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM MONILIFORME fusarium moniliforme solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1670
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1670-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1670-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS FUMIGATUS aspergillus fumigatus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1619
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 0.002 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1619-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS FLAVUS aspergillus flavus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5603
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FLAVUS (ASPERGILLUS FLAVUS) ASPERGILLUS FLAVUS 0.025 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5603-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5603-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5603-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
BIPOLARIS SOROKINIANA bipolaris sorokiniana solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1634
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1634-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1634-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CLADOSPORIUM HERBARUM cladosporium herbarum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1657
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM HERBARUM (CLADOSPORIUM HERBARUM) CLADOSPORIUM HERBARUM 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1657-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CANDIDA ALBICANS candida albicans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1640
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 0.01 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1640-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CANDIDA ALBICANS candida albicans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1642
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1642-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS AMSTELODAMI aspergillus amstelodami solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5602
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EUROTIUM AMSTELODAMI (EUROTIUM AMSTELODAMI) EUROTIUM AMSTELODAMI 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5602-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5602-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5602-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS NIGER aspergillus niger solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5606
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5606-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5606-5 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CANDIDA ALBICANS candida albicans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1644
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1644-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1644-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
EPICOCCUM NIGRUM epicoccum nigrum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1666
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EPICOCCUM NIGRUM (EPICOCCUM NIGRUM) EPICOCCUM NIGRUM 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1666-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS NIGER aspergillus niger solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1628
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1628-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
BIPOLARIS SOROKINIANA bipolaris sorokiniana solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1633
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1633-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1633-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
DRECHSLERA SPICIFERA drechslera spicifera solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5615
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SPICIFER (COCHLIOBOLUS SPICIFER) COCHLIOBOLUS SPICIFER 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5615-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5615-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5615-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM SOLANI fusarium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1676
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HAEMATONECTRIA HAEMATOCOCCA (HAEMATONECTRIA HAEMATOCOCCA) HAEMATONECTRIA HAEMATOCOCCA 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1676-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM SOLANI fusarium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5619
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HAEMATONECTRIA HAEMATOCOCCA (HAEMATONECTRIA HAEMATOCOCCA) HAEMATONECTRIA HAEMATOCOCCA 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5619-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5619-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
GLIOCLADIUM VIRIDE gliocladium viride solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1681
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GLIOCLADIUM VIRIDE (GLIOCLADIUM VIRIDE) GLIOCLADIUM VIRIDE 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1681-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1681-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
GLIOCLADIUM VIRIDE gliocladium viride solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1682
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GLIOCLADIUM VIRIDE (GLIOCLADIUM VIRIDE) GLIOCLADIUM VIRIDE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1682-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
HELMINTHOSPORIUM SOLANI helminthosporium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1691
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HELMINTHOSPORIUM SOLANI (HELMINTHOSPORIUM SOLANI) HELMINTHOSPORIUM SOLANI 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1691-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1691-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
HELMINTHOSPORIUM SOLANI helminthosporium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2668
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HELMINTHOSPORIUM SOLANI (HELMINTHOSPORIUM SOLANI) HELMINTHOSPORIUM SOLANI 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2668-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2668-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
HELMINTHOSPORIUM SOLANI helminthosporium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5622
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HELMINTHOSPORIUM SOLANI (HELMINTHOSPORIUM SOLANI) HELMINTHOSPORIUM SOLANI 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5622-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5622-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5622-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR PLUMBEUS mucor plumbeus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1694
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1694-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1694-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHIZOPUS ORYZAE rhizopus oryzae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5633
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS ARRHIZUS (RHIZOPUS ARRHIZUS) RHIZOPUS ARRHIZUS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5633-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
STEMPHYLIUM SOLANI stemphylium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2637
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
STEMPHYLIUM SOLANI (STEMPHYLIUM SOLANI) STEMPHYLIUM SOLANI 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2637-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2637-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
STEMPHYLIUM SOLANI stemphylium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2636
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
STEMPHYLIUM SOLANI (STEMPHYLIUM SOLANI) STEMPHYLIUM SOLANI 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2636-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
STEMPHYLIUM SOLANI stemphylium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5637
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
STEMPHYLIUM SOLANI (STEMPHYLIUM SOLANI) STEMPHYLIUM SOLANI 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5637-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5637-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHODERMA HARZIANUM trichoderma harzianum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2642
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHODERMA HARZIANUM (TRICHODERMA HARZIANUM) TRICHODERMA HARZIANUM 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2642-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR CIRCINELLOIDES F. LUSITANICUS mucor circinelloides f. lusitanicus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5625
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (MUCOR CIRCINELLOIDES F. LUSITANICUS) MUCOR CIRCINELLOIDES F. LUSITANICUS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5625-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CHAETOMIUM GLOBOSUM chaetomium globosum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5612
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHAETOMIUM GLOBOSUM (CHAETOMIUM GLOBOSUM) CHAETOMIUM GLOBOSUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5612-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5612-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CLADOSPORIUM SPHAEROSPERMUM cladosporium sphaerospermum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2663
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2663-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CLADOSPORIUM SPHAEROSPERMUM cladosporium sphaerospermum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5614
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5614-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5614-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5614-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES mucor circinelloides f. circinelloides solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2669
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (MUCOR CIRCINELLOIDES F. CIRCINELLOIDES) MUCOR CIRCINELLOIDES F. CIRCINELLOIDES 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2669-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PENICILLIUM CHRYSOGENUM (NOTATUM) penicillium chrysogenum (notatum) solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5631
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5631-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5631-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHODERMA HARZIANUM trichoderma harzianum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2640
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHODERMA HARZIANUM (TRICHODERMA HARZIANUM) TRICHODERMA HARZIANUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2640-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2640-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 3 alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9616
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 5000 [PNU] in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 5000 [PNU] in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 5000 [PNU] in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 5000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9616-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9616-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 3 alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9617
Route of Administration INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.025 g in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.025 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.025 g in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9617-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9617-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ALTERNARIA/HORMODENDRUM MIX alternaria alternata and aspergillus fumigatus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9674
Route of Administration INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 10000 [PNU] in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9674-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9674-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ACREMONIUM STRICTUM acremonium strictum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5601
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SAROCLADIUM STRICTUM (SAROCLADIUM STRICTUM) SAROCLADIUM STRICTUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5601-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5601-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS NIGER aspergillus niger solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1627
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1627-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 3 alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9619
Route of Administration INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.0125 g in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.0125 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.0125 g in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.0125 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9619-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MONILIA MIX candida albicans and neurospora intermedia solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9642
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 10000 [PNU] in 1 mL
NEUROSPORA INTERMEDIA (NEUROSPORA INTERMEDIA) NEUROSPORA INTERMEDIA 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9642-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9642-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
NEW STOCK FUNGI MIX acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9653
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.003125 g in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.003125 g in 1 mL
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 0.003125 g in 1 mL
CHAETOMIUM GLOBOSUM (CHAETOMIUM GLOBOSUM) CHAETOMIUM GLOBOSUM 0.003125 g in 1 mL
TRICHOPHYTON MENTAGROPHYTES (TRICHOPHYTON MENTAGROPHYTES) TRICHOPHYTON MENTAGROPHYTES 0.003125 g in 1 mL
EPICOCCUM NIGRUM (EPICOCCUM NIGRUM) EPICOCCUM NIGRUM 0.003125 g in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.003125 g in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.003125 g in 1 mL
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.003125 g in 1 mL
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.003125 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.003125 g in 1 mL
ACREMONIUM STRICTUM (ACREMONIUM STRICTUM) ACREMONIUM STRICTUM 0.003125 g in 1 mL
BOTRYTIS CINEREA (BOTRYTIS CINEREA) BOTRYTIS CINEREA 0.003125 g in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.003125 g in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.003125 g in 1 mL
PLEOSPORA BETAE (PLEOSPORA BETAE) PLEOSPORA BETAE 0.003125 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9653-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9653-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-9653-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
GRAIN SMUT MIX ustilago maydis, ustilago tritici, ustilago nuda and ustilago avenae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9670
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
USTILAGO NUDA (USTILAGO NUDA) USTILAGO NUDA 0.00625 g in 1 mL
USTILAGO AVENAE (USTILAGO AVENAE) USTILAGO AVENAE 0.00625 g in 1 mL
USTILAGO MAYDIS (USTILAGO MAYDIS) USTILAGO MAYDIS 0.00625 g in 1 mL
USTILAGO TRITICI (USTILAGO TRITICI) USTILAGO TRITICI 0.00625 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9670-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9670-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-9670-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
NEUROSPORA INTERMEDIA neurospora intermedia solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2600
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NEUROSPORA INTERMEDIA (NEUROSPORA INTERMEDIA) NEUROSPORA INTERMEDIA 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2600-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2600-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
NEUROSPORA INTERMEDIA neurospora intermedia solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5627
Route of Administration SUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NEUROSPORA INTERMEDIA (NEUROSPORA INTERMEDIA) NEUROSPORA INTERMEDIA 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5627-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5627-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PAECILOMYCES VARIOTII paecilomyces variotii solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2605
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PAECILOMYCES VARIOTII (PAECILOMYCES VARIOTII) PAECILOMYCES VARIOTII 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2605-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2605-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PENICILLIUM DIGITATUM penicillium digitatum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5630
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM DIGITATUM (PENICILLIUM DIGITATUM) PENICILLIUM DIGITATUM 0.0125 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5630-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5630-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PENICILLIUM CHRYSOGENUM (NOTATUM) penicillium chrysogenum (notatum) solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2615
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2615-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PHOMA BETAE phoma betae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5632
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PLEOSPORA BETAE (PLEOSPORA BETAE) PLEOSPORA BETAE 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5632-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5632-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHIZOPUS ORYZAE rhizopus oryzae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2619
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS ARRHIZUS (RHIZOPUS ARRHIZUS) RHIZOPUS ARRHIZUS 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2619-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS MIX aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9627
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.02 g in 1 mL
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 0.02 g in 1 mL
EUROTIUM AMSTELODAMI (EUROTIUM AMSTELODAMI) EUROTIUM AMSTELODAMI 0.02 g in 1 mL
ASPERGILLUS FLAVUS (ASPERGILLUS FLAVUS) ASPERGILLUS FLAVUS 0.02 g in 1 mL
ASPERGILLUS NIDULANS (ASPERGILLUS NIDULANS) ASPERGILLUS NIDULANS 0.02 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9627-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9627-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ALTERNARIA ALTERNATA alternaria alternata solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1604
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1604-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ACREMONIUM STRICTUM acremonium strictum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1606
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SAROCLADIUM STRICTUM (SAROCLADIUM STRICTUM) SAROCLADIUM STRICTUM 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1606-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHIZOPUS STOLONIFER rhizopus stolonifer solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2623
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2623-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2623-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR CIRCINELLOIDES F. LUSITANICUS mucor circinelloides f. lusitanicus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2671
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (MUCOR CIRCINELLOIDES F. LUSITANICUS) MUCOR CIRCINELLOIDES F. LUSITANICUS 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2671-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOTHECIUM ROSEUM trichothecium roseum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2654
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOTHECIUM ROSEUM (TRICHOTHECIUM ROSEUM) TRICHOTHECIUM ROSEUM 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2654-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2654-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOTHECIUM ROSEUM trichothecium roseum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2656
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOTHECIUM ROSEUM (TRICHOTHECIUM ROSEUM) TRICHOTHECIUM ROSEUM 1000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2656-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MYCOGONE PERNICIOSA mycogone perniciosa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5642
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HYPOMYCES PERNICIOSUS (HYPOMYCES PERNICIOSUS) HYPOMYCES PERNICIOSUS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5642-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5642-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5642-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ALTERNARIA ALTERNATA alternaria alternata solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1600
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1600-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1600-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ALTERNARIA ALTERNATA alternaria alternata solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1601
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1601-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1601-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS FLAVUS aspergillus flavus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1610
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FLAVUS (ASPERGILLUS FLAVUS) ASPERGILLUS FLAVUS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1610-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1610-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS FUMIGATUS aspergillus fumigatus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1615
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1615-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1615-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS NIGER aspergillus niger solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1625
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1625-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1625-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CHAETOMIUM GLOBOSUM chaetomium globosum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1648
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHAETOMIUM GLOBOSUM (CHAETOMIUM GLOBOSUM) CHAETOMIUM GLOBOSUM 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1648-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1648-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CHAETOMIUM GLOBOSUM chaetomium globosum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1647
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHAETOMIUM GLOBOSUM (CHAETOMIUM GLOBOSUM) CHAETOMIUM GLOBOSUM 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1647-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1647-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CHAETOMIUM GLOBOSUM chaetomium globosum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1650
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHAETOMIUM GLOBOSUM (CHAETOMIUM GLOBOSUM) CHAETOMIUM GLOBOSUM 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1650-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CHAETOMIUM GLOBOSUM chaetomium globosum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1651
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHAETOMIUM GLOBOSUM (CHAETOMIUM GLOBOSUM) CHAETOMIUM GLOBOSUM 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1651-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 3 alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9614
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.00025 g in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.00025 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.00025 g in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.00025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9614-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 3 alternaria alternata, aspergillus niger, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9618
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 10000 [PNU] in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 10000 [PNU] in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 10000 [PNU] in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9618-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS MIX aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9631
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.0002 g in 1 mL
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 0.0002 g in 1 mL
EUROTIUM AMSTELODAMI (EUROTIUM AMSTELODAMI) EUROTIUM AMSTELODAMI 0.0002 g in 1 mL
ASPERGILLUS FLAVUS (ASPERGILLUS FLAVUS) ASPERGILLUS FLAVUS 0.0002 g in 1 mL
ASPERGILLUS NIDULANS (ASPERGILLUS NIDULANS) ASPERGILLUS NIDULANS 0.0002 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9631-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
DEMATIACEAE MIX alternaria alternata, aureobasidium pullulans, bipolaris sorokiniana, cladosporium herbarum, curvularia spicifera and helminthosporium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9634
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SPICIFER (COCHLIOBOLUS SPICIFER) COCHLIOBOLUS SPICIFER 0.0083 g in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.0083 g in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.0083 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.0083 g in 1 mL
CLADOSPORIUM HERBARUM (CLADOSPORIUM HERBARUM) CLADOSPORIUM HERBARUM 0.0083 g in 1 mL
HELMINTHOSPORIUM SOLANI (HELMINTHOSPORIUM SOLANI) HELMINTHOSPORIUM SOLANI 0.0083 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9634-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
NEW STOCK FUNGI MIX acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9649
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.00625 g in 1 mL
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.00625 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.00625 g in 1 mL
ACREMONIUM STRICTUM (ACREMONIUM STRICTUM) ACREMONIUM STRICTUM 0.00625 g in 1 mL
BOTRYTIS CINEREA (BOTRYTIS CINEREA) BOTRYTIS CINEREA 0.00625 g in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.00625 g in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.00625 g in 1 mL
PLEOSPORA BETAE (PLEOSPORA BETAE) PLEOSPORA BETAE 0.00625 g in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.00625 g in 1 mL
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 0.00625 g in 1 mL
CHAETOMIUM GLOBOSUM (CHAETOMIUM GLOBOSUM) CHAETOMIUM GLOBOSUM 0.00625 g in 1 mL
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.00625 g in 1 mL
TRICHOPHYTON MENTAGROPHYTES (TRICHOPHYTON MENTAGROPHYTES) TRICHOPHYTON MENTAGROPHYTES 0.00625 g in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.00625 g in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.00625 g in 1 mL
EPICOCCUM NIGRUM (EPICOCCUM NIGRUM) EPICOCCUM NIGRUM 0.00625 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9649-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9649-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
NEW STOCK FUNGI MIX acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9652
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.003125 g in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.003125 g in 1 mL
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 0.003125 g in 1 mL
CHAETOMIUM GLOBOSUM (CHAETOMIUM GLOBOSUM) CHAETOMIUM GLOBOSUM 0.003125 g in 1 mL
TRICHOPHYTON MENTAGROPHYTES (TRICHOPHYTON MENTAGROPHYTES) TRICHOPHYTON MENTAGROPHYTES 0.003125 g in 1 mL
EPICOCCUM NIGRUM (EPICOCCUM NIGRUM) EPICOCCUM NIGRUM 0.003125 g in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.003125 g in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.003125 g in 1 mL
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.003125 g in 1 mL
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.003125 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.003125 g in 1 mL
ACREMONIUM STRICTUM (ACREMONIUM STRICTUM) ACREMONIUM STRICTUM 0.003125 g in 1 mL
BOTRYTIS CINEREA (BOTRYTIS CINEREA) BOTRYTIS CINEREA 0.003125 g in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.003125 g in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.003125 g in 1 mL
PLEOSPORA BETAE (PLEOSPORA BETAE) PLEOSPORA BETAE 0.003125 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9652-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
GRASS SMUT MIX ustilago cynodontis and sporisorium cruentum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9676
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
USTILAGO CYNODONTIS (USTILAGO CYNODONTIS) USTILAGO CYNODONTIS 0.05 g in 1 mL
SPORISORIUM CRUENTUM (SPORISORIUM CRUENTUM) SPORISORIUM CRUENTUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9676-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
DRECHSLERA SPICIFERA drechslera spicifera solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1664
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SPICIFER (COCHLIOBOLUS SPICIFER) COCHLIOBOLUS SPICIFER 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1664-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
DRECHSLERA SPICIFERA drechslera spicifera solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1662
Route of Administration INTRADERMAL, SUBCUTANEOUS, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SPICIFER (COCHLIOBOLUS SPICIFER) COCHLIOBOLUS SPICIFER 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1662-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ALTERNARIA HORMODENDRUM MIX alternaria alternata and aspergillus fumigatus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9626
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.025 g in 1 mL
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9626-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9626-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
HELMINTHOSPORIUM SOLANI helminthosporium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1690
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HELMINTHOSPORIUM SOLANI (HELMINTHOSPORIUM SOLANI) HELMINTHOSPORIUM SOLANI 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1690-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR PLUMBEUS mucor plumbeus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1696
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1696-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR PLUMBEUS mucor plumbeus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5626
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
GLYCERIN
SODIUM BICARBONATE
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5626-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5626-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS NIDULANS aspergillus nidulans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1622
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIDULANS (ASPERGILLUS NIDULANS) ASPERGILLUS NIDULANS 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1622-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1622-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS NIDULANS aspergillus nidulans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2660
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIDULANS (ASPERGILLUS NIDULANS) ASPERGILLUS NIDULANS 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2660-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
AUREOBASIDIUM PULLULANS aureobasidium pullulans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1630
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1630-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
BIPOLARIS SOROKINIANA bipolaris sorokiniana solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1635
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1635-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1635-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
BIPOLARIS SOROKINIANA bipolaris sorokiniana solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1636
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.01 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1636-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
BIPOLARIS SOROKINIANA bipolaris sorokiniana solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5608
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5608-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5608-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5608-5 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS FUMIGATUS aspergillus fumigatus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1617
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1617-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1617-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS FUMIGATUS aspergillus fumigatus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1618
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1618-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1618-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
NEW STOCK FUNGI MIX acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9650
Route of Administration SUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.0000625 g in 1 mL
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.0000625 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.0000625 g in 1 mL
ACREMONIUM STRICTUM (ACREMONIUM STRICTUM) ACREMONIUM STRICTUM 0.0000625 g in 1 mL
BOTRYTIS CINEREA (BOTRYTIS CINEREA) BOTRYTIS CINEREA 0.0000625 g in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.0000625 g in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.0000625 g in 1 mL
PLEOSPORA BETAE (PLEOSPORA BETAE) PLEOSPORA BETAE 0.0000625 g in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.0000625 g in 1 mL
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 0.0000625 g in 1 mL
CHAETOMIUM GLOBOSUM (CHAETOMIUM GLOBOSUM) CHAETOMIUM GLOBOSUM 0.0000625 g in 1 mL
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.0000625 g in 1 mL
TRICHOPHYTON MENTAGROPHYTES (TRICHOPHYTON MENTAGROPHYTES) TRICHOPHYTON MENTAGROPHYTES 0.0000625 g in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.0000625 g in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.0000625 g in 1 mL
EPICOCCUM NIGRUM (EPICOCCUM NIGRUM) EPICOCCUM NIGRUM 0.0000625 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9650-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PENICILLIUM MIX penicillium camemberti, penicillium chrysogenum, penicillium digitatum, penicillium notatum and penicillium roqueforti solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9654
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM DIGITATUM (PENICILLIUM DIGITATUM) PENICILLIUM DIGITATUM 0.025 g in 1 mL
PENICILLIUM CAMEMBERTI (PENICILLIUM CAMEMBERTI) PENICILLIUM CAMEMBERTI 0.025 g in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.025 g in 1 mL
PENICILLIUM ROQUEFORTI (PENICILLIUM ROQUEFORTI) PENICILLIUM ROQUEFORTI 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9654-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9654-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981 10/01/2019
GRASS SMUT MIX ustilago cynodontis and sporisorium cruentum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9671
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
USTILAGO CYNODONTIS (USTILAGO CYNODONTIS) USTILAGO CYNODONTIS 0.05 g in 1 mL
SPORISORIUM CRUENTUM (SPORISORIUM CRUENTUM) SPORISORIUM CRUENTUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9671-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9671-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-9671-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
GRAIN SMUT MIX ustilago maydis, ustilago tritici, ustilago nuda and ustilago avenae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9675
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
USTILAGO NUDA (USTILAGO NUDA) USTILAGO NUDA 0.0125 g in 1 mL
USTILAGO AVENAE (USTILAGO AVENAE) USTILAGO AVENAE 0.0125 g in 1 mL
USTILAGO MAYDIS (USTILAGO MAYDIS) USTILAGO MAYDIS 0.0125 g in 1 mL
USTILAGO TRITICI (USTILAGO TRITICI) USTILAGO TRITICI 0.0125 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9675-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CANDIDA ALBICANS candida albicans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1641
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1641-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1641-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CORN SMUT ustilago maydis solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2664
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
USTILAGO MAYDIS (USTILAGO MAYDIS) USTILAGO MAYDIS 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2664-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CANDIDA ALBICANS candida albicans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1643
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1643-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
EPIDERMOPHYTON FLOCCOSUM epidermophyton floccosum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1667
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EPIDERMOPHYTON FLOCCOSUM (EPIDERMOPHYTON FLOCCOSUM) EPIDERMOPHYTON FLOCCOSUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1667-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1667-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
EPIDERMOPHYTON FLOCCOSUM epidermophyton floccosum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1669
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EPIDERMOPHYTON FLOCCOSUM (EPIDERMOPHYTON FLOCCOSUM) EPIDERMOPHYTON FLOCCOSUM 1000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1669-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CLADOSPORIUM SPHAEROSPERMUM cladosporium sphaerospermum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1659
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1659-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
DRECHSLERA SPICIFERA drechslera spicifera solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1661
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SPICIFER (COCHLIOBOLUS SPICIFER) COCHLIOBOLUS SPICIFER 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1661-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1661-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PAECILOMYCES VARIOTII paecilomyces variotii solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2606
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PAECILOMYCES VARIOTII (PAECILOMYCES VARIOTII) PAECILOMYCES VARIOTII 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2606-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2606-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHODERMA HARZIANUM trichoderma harzianum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5638
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHODERMA HARZIANUM (TRICHODERMA HARZIANUM) TRICHODERMA HARZIANUM 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5638-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5638-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5638-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOPHYTON MENTAGROPHYTES trichophyton mentagrophytes solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2645
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOPHYTON MENTAGROPHYTES (TRICHOPHYTON MENTAGROPHYTES) TRICHOPHYTON MENTAGROPHYTES 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2645-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2645-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM MONILIFORME fusarium moniliforme solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1673
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1673-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM SOLANI fusarium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1678
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HAEMATONECTRIA HAEMATOCOCCA (HAEMATONECTRIA HAEMATOCOCCA) HAEMATONECTRIA HAEMATOCOCCA 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1678-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 1 alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9601
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 4000 [PNU] in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 4000 [PNU] in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 4000 [PNU] in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 4000 [PNU] in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 4000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9601-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9601-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM MONILIFORME fusarium moniliforme solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1674
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1674-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM SOLANI fusarium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1677
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HAEMATONECTRIA HAEMATOCOCCA (HAEMATONECTRIA HAEMATOCOCCA) HAEMATONECTRIA HAEMATOCOCCA 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1677-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
GEOTRICHUM CANDIDUM geotrichum candidum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1680
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GEOTRICHUM CANDIDUM (GEOTRICHUM CANDIDUM) GEOTRICHUM CANDIDUM 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1680-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
GLIOCLADIUM VIRIDE gliocladium viride solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5621
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GLIOCLADIUM VIRIDE (GLIOCLADIUM VIRIDE) GLIOCLADIUM VIRIDE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5621-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5621-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5621-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR PLUMBEUS mucor plumbeus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1698
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1698-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
NEUROSPORA INTERMEDIA neurospora intermedia solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2601
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NEUROSPORA INTERMEDIA (NEUROSPORA INTERMEDIA) NEUROSPORA INTERMEDIA 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2601-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PAECILOMYCES VARIOTII paecilomyces variotii solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2609
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PAECILOMYCES VARIOTII (PAECILOMYCES VARIOTII) PAECILOMYCES VARIOTII 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2609-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2609-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PAECILOMYCES VARIOTII paecilomyces variotii solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5629
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PAECILOMYCES VARIOTII (PAECILOMYCES VARIOTII) PAECILOMYCES VARIOTII 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5629-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5629-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5629-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PENICILLIUM CHRYSOGENUM (NOTATUM) penicillium chrysogenum (notatum) solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2614
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2614-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2614-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PHOMA BETAE phoma betae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2674
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PLEOSPORA BETAE (PLEOSPORA BETAE) PLEOSPORA BETAE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2674-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES mucor circinelloides f. circinelloides solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5624
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR CIRCINELLOIDES F. CIRCINELLOIDES (MUCOR CIRCINELLOIDES F. CIRCINELLOIDES) MUCOR CIRCINELLOIDES F. CIRCINELLOIDES 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5624-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5624-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
PAECILOMYCES VARIOTII paecilomyces variotii solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2607
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PAECILOMYCES VARIOTII (PAECILOMYCES VARIOTII) PAECILOMYCES VARIOTII 1000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2607-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS FUMIGATUS aspergillus fumigatus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1621
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1621-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHIZOPUS STOLONIFER rhizopus stolonifer solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2624
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2624-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2624-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHIZOPUS STOLONIFER rhizopus stolonifer solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2625
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2625-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
SACCHAROMYCES CEREVISIAE saccharomyces cerevisiae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2634
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SACCHAROMYCES CEREVISIAE (SACCHAROMYCES CEREVISIAE) SACCHAROMYCES CEREVISIAE 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2634-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-2634-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
SACCHAROMYCES CEREVISIAE saccharomyces cerevisiae solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2677
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SACCHAROMYCES CEREVISIAE (SACCHAROMYCES CEREVISIAE) SACCHAROMYCES CEREVISIAE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2677-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOPHYTON MENTAGROPHYTES trichophyton mentagrophytes solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2646
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOPHYTON MENTAGROPHYTES (TRICHOPHYTON MENTAGROPHYTES) TRICHOPHYTON MENTAGROPHYTES 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2646-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
TRICHOPHYTON RUBRUM trichophyton rubrum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5640
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOPHYTON RUBRUM (TRICHOPHYTON RUBRUM) TRICHOPHYTON RUBRUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5640-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5640-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 1 alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9602
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 8000 [PNU] in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 8000 [PNU] in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 8000 [PNU] in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 8000 [PNU] in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 8000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9602-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9602-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 1 alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9604
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.0002 g in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.0002 g in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.0002 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.0002 g in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.0002 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9604-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 1 alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9606
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.01 g in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.01 g in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.01 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.01 g in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.01 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9606-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9606-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-9606-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 2 aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9608
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 4000 [PNU] in 1 mL
COCHLIOBOLUS SPICIFER (COCHLIOBOLUS SPICIFER) COCHLIOBOLUS SPICIFER 4000 [PNU] in 1 mL
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 4000 [PNU] in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 4000 [PNU] in 1 mL
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 4000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9608-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9608-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ACREMONIUM STRICTUM acremonium strictum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2679
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SAROCLADIUM STRICTUM (SAROCLADIUM STRICTUM) SAROCLADIUM STRICTUM 0.1 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2679-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
BOTRYTIS CINEREA botrytis cinerea solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5609
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BOTRYTIS CINEREA (BOTRYTIS CINEREA) BOTRYTIS CINEREA 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5609-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5609-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CANDIDA ALBICANS candida albicans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1646
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1646-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHIZOPUS STOLONIFER rhizopus stolonifer solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2627
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2627-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHIZOPUS STOLONIFER rhizopus stolonifer solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5634
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5634-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5634-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
RHODOTORULA MUCILAGINOSA rhodotorula mucilaginosa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2628
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHODOTORULA MUCILAGINOSA (RHODOTORULA MUCILAGINOSA) RHODOTORULA MUCILAGINOSA 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2628-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CANDIDA ALBICANS candida albicans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5610
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5610-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5610-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
CLADOSPORIUM HERBARUM cladosporium herbarum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5613
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM HERBARUM (CLADOSPORIUM HERBARUM) CLADOSPORIUM HERBARUM 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5613-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5613-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 1 alternaria alternata, aspergillus niger, bipolaris sorokiniana, cladosporium sphaerospermum and penicillium notatum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9600
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.02 g in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.02 g in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.02 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.02 g in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.02 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9600-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9600-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
GLIOCLADIUM VIRIDE gliocladium viride solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1683
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GLIOCLADIUM VIRIDE (GLIOCLADIUM VIRIDE) GLIOCLADIUM VIRIDE 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1683-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
GLIOCLADIUM VIRIDE gliocladium viride solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1684
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GLIOCLADIUM VIRIDE (GLIOCLADIUM VIRIDE) GLIOCLADIUM VIRIDE 1000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1684-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 2 aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9612
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 0.0002 g in 1 mL
COCHLIOBOLUS SPICIFER (COCHLIOBOLUS SPICIFER) COCHLIOBOLUS SPICIFER 0.0002 g in 1 mL
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.0002 g in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.0002 g in 1 mL
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.0002 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9612-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
AHH MOLD MIX alternaria alternata, bipolaris sorokiniana and cladosporium sphaerospermum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9622
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.00033 g in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.00033 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.00033 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9622-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
AHH MOLD MIX alternaria alternata, bipolaris sorokiniana and cladosporium sphaerospermum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9673
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 13333.333 [PNU] in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 13333.333 [PNU] in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 13333.333 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9673-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
AHH MOLD MIX alternaria alternata, bipolaris sorokiniana and cladosporium sphaerospermum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9623
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.0166 g in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.0166 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.0166 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9623-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9623-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
AHH MOLD MIX alternaria alternata, bipolaris sorokiniana and cladosporium sphaerospermum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9621
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.0166 g in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.0166 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.0166 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9621-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9621-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ALTERNARIA/HORMODENDRUM MIX alternaria alternata and aspergillus fumigatus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9624
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 0.025 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9624-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS MIX aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9630
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.01 g in 1 mL
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 0.01 g in 1 mL
EUROTIUM AMSTELODAMI (EUROTIUM AMSTELODAMI) EUROTIUM AMSTELODAMI 0.01 g in 1 mL
ASPERGILLUS FLAVUS (ASPERGILLUS FLAVUS) ASPERGILLUS FLAVUS 0.01 g in 1 mL
ASPERGILLUS NIDULANS (ASPERGILLUS NIDULANS) ASPERGILLUS NIDULANS 0.01 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9630-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
DEMATIACEAE MIX alternaria alternata, aureobasidium pullulans, bipolaris sorokiniana, cladosporium herbarum, curvularia spicifera and helminthosporium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9635
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SPICIFER (COCHLIOBOLUS SPICIFER) COCHLIOBOLUS SPICIFER 0.0042 g in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.0042 g in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.0042 g in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.0042 g in 1 mL
CLADOSPORIUM HERBARUM (CLADOSPORIUM HERBARUM) CLADOSPORIUM HERBARUM 0.0042 g in 1 mL
HELMINTHOSPORIUM SOLANI (HELMINTHOSPORIUM SOLANI) HELMINTHOSPORIUM SOLANI 0.0042 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9635-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9635-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS NIDULANS aspergillus nidulans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1623
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIDULANS (ASPERGILLUS NIDULANS) ASPERGILLUS NIDULANS 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1623-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
ASPERGILLUS MIX aspergillus amstelodami, aspergillus flavus, aspergillus fumigatus, aspergillus nidulans and aspergillus niger solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9629
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 4000 [PNU] in 1 mL
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 4000 [PNU] in 1 mL
EUROTIUM AMSTELODAMI (EUROTIUM AMSTELODAMI) EUROTIUM AMSTELODAMI 4000 [PNU] in 1 mL
ASPERGILLUS FLAVUS (ASPERGILLUS FLAVUS) ASPERGILLUS FLAVUS 4000 [PNU] in 1 mL
ASPERGILLUS NIDULANS (ASPERGILLUS NIDULANS) ASPERGILLUS NIDULANS 4000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9629-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9629-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
EPICOCCUM NIGRUM epicoccum nigrum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-2665
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EPICOCCUM NIGRUM (EPICOCCUM NIGRUM) EPICOCCUM NIGRUM 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-2665-2 10 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
EPIDERMOPHYTON FLOCCOSUM epidermophyton floccosum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1668
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EPIDERMOPHYTON FLOCCOSUM (EPIDERMOPHYTON FLOCCOSUM) EPIDERMOPHYTON FLOCCOSUM 0.001 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1668-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM MIX gibberella fujikuroi and fusarium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9636
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HAEMATONECTRIA HAEMATOCOCCA (HAEMATONECTRIA HAEMATOCOCCA) HAEMATONECTRIA HAEMATOCOCCA 0.025 g in 1 mL
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9636-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9636-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM MIX gibberella fujikuroi and fusarium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9637
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HAEMATONECTRIA HAEMATOCOCCA (HAEMATONECTRIA HAEMATOCOCCA) HAEMATONECTRIA HAEMATOCOCCA 20000 [PNU] in 1 mL
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9637-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9637-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM MIX gibberella fujikuroi and fusarium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9638
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HAEMATONECTRIA HAEMATOCOCCA (HAEMATONECTRIA HAEMATOCOCCA) HAEMATONECTRIA HAEMATOCOCCA 10000 [PNU] in 1 mL
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9638-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM MIX gibberella fujikuroi and fusarium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9639
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HAEMATONECTRIA HAEMATOCOCCA (HAEMATONECTRIA HAEMATOCOCCA) HAEMATONECTRIA HAEMATOCOCCA 0.0005 g in 1 mL
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.0005 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9639-1 5 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
FUSARIUM MIX gibberella fujikuroi and fusarium solani solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9641
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HAEMATONECTRIA HAEMATOCOCCA (HAEMATONECTRIA HAEMATOCOCCA) HAEMATONECTRIA HAEMATOCOCCA 0.0125 g in 1 mL
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 0.0125 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9641-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9641-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-9641-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MUCOR MIX mucor circinelloides f. lusitanicus and mucor plumbeus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9648
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR CIRCINELLOIDES F. LUSITANICUS (MUCOR CIRCINELLOIDES F. LUSITANICUS) MUCOR CIRCINELLOIDES F. LUSITANICUS 0.025 g in 1 mL
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9648-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9648-5 5 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
NEW STOCK FUNGI MIX acremonium strictum, alternaria alternata, aspergillus niger, aureobasidium pullulans, bipolaris sorokiniana, botrytis cinerea, candida albicans, chaetomium globosum, cladosporium sphaerospermum, epicoccum nigrum, gibberella fujikuroi, mucor plumbeus, penicillium notatum, phoma betae, rhizopus stolonifer and trichophyton mentagrophytes solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9651
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PLEOSPORA BETAE (PLEOSPORA BETAE) PLEOSPORA BETAE 1250 [PNU] in 1 mL
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 1250 [PNU] in 1 mL
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 1250 [PNU] in 1 mL
CHAETOMIUM GLOBOSUM (CHAETOMIUM GLOBOSUM) CHAETOMIUM GLOBOSUM 1250 [PNU] in 1 mL
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 1250 [PNU] in 1 mL
TRICHOPHYTON MENTAGROPHYTES (TRICHOPHYTON MENTAGROPHYTES) TRICHOPHYTON MENTAGROPHYTES 1250 [PNU] in 1 mL
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 1250 [PNU] in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 1250 [PNU] in 1 mL
EPICOCCUM NIGRUM (EPICOCCUM NIGRUM) EPICOCCUM NIGRUM 1250 [PNU] in 1 mL
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 1250 [PNU] in 1 mL
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 1250 [PNU] in 1 mL
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 1250 [PNU] in 1 mL
ACREMONIUM STRICTUM (ACREMONIUM STRICTUM) ACREMONIUM STRICTUM 1250 [PNU] in 1 mL
BOTRYTIS CINEREA (BOTRYTIS CINEREA) BOTRYTIS CINEREA 1250 [PNU] in 1 mL
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 1250 [PNU] in 1 mL
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 1250 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9651-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9651-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA101833 09/15/1981
MOLD MIX 2 aureobasidium pullulans, curvularia spicifera, gibberella fujikuroi, mucor plumbeus and rhizopus stolonifer solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9610
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS STOLONIFER (RHIZOPUS STOLONIFER) RHIZOPUS STOLONIFER 8000 [PNU] in 1 mL
COCHLIOBOLUS SPICIFER (COCHLIOBOLUS SPICIFER) COCHLIOBOLUS SPICIFER 8000 [PNU] in 1 mL
GIBBERELLA FUJIKUROI (GIBBERELLA FUJIKUROI) GIBBERELLA FUJIKUROI 8000 [PNU] in 1 mL
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 8000 [PNU] in 1 mL
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 8000 [PNU] in 1 mL
Inactive Ingredients
Ing