Rice Food: Package Insert and Label Information (Page 3 of 3)

17 PATIENT COUNSELING INFORMATION

Instruct patient to remain under observation in the office for 30 minutes or longer after an injection.

Caution patient that reactions can occur more than 30 minutes after skin testing or an injection.

Instruct patient to recognize the following symptoms as adverse reactions and to immediately return to the office or immediately seek other medical attention if any of these symptoms occur following skin testing or an injection:

  • Unusual swelling and/or tenderness at the injection site
  • Hives or itching of the skin
  • Swelling of the face and/or mouth
  • Sneezing, coughing or wheezing
  • Shortness of breath
  • Nausea
  • Dizziness or faintness

Manufacturer:

U.S. License No. 308

Greer Laboratories, Inc.

Lenoir, NC 28645 U.S.A

5786-5_Peanut_20-wv
(click image for full-size original)

5765-2_Cow_Milk_20-wv
(click image for full-size original)
RICE FOOD oryza sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5746
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BROWN RICE (BROWN RICE) BROWN RICE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5746-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5746-2 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
RYE FOOD secale cereale solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5747
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RYE (RYE) RYE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5747-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5747-2 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
SESAME SEED sesamum indicum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5748
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SESAME SEED (SESAME SEED) SESAME SEED 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5748-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5748-2 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
BROCCOLI brassica oleracea var. botrytis solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5708
Route of Administration SUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BROCCOLI (BROCCOLI) BROCCOLI 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:22840-5708-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5708-2 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
BUCKWHEAT fagopyrum esculentum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5709
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BUCKWHEAT (BUCKWHEAT) BUCKWHEAT 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5709-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5709-2 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
CASHEW NUT anacardium occidentale solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5783
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ANACARDIUM OCCIDENTALE FRUIT (ANACARDIUM OCCIDENTALE FRUIT) ANACARDIUM OCCIDENTALE FRUIT 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:22840-5783-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5783-5 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
CAULIFLOWER brassica oleracea var. botrytis solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5713
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CAULIFLOWER (CAULIFLOWER) CAULIFLOWER 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5713-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5713-2 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
CHOCOLATE CACAO BEAN theobroma cacao solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5716
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
THEOBROMA CACAO WHOLE (THEOBROMA CACAO WHOLE) THEOBROMA CACAO WHOLE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5716-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5716-2 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
CANTALOUPE MUSKMELON cucumis melo solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5711
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUSKMELON (MUSKMELON) MUSKMELON 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5711-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5711-2 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
CARROT daucus carota solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5712
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CARROT (CARROT) CARROT 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:22840-5712-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5712-2 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
CELERY apium graveolens var. dulce solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5714
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CELERY (CELERY) CELERY 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:22840-5714-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5714-2 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
LETTUCE lactuca sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5728
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LACTUCA SATIVA WHOLE (LACTUCA SATIVA WHOLE) LACTUCA SATIVA WHOLE 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:22840-5728-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5728-2 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
FILBERT HAZELNUT FOOD corylus americana solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5785
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AMERICAN HAZELNUT (AMERICAN HAZELNUT) AMERICAN HAZELNUT 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:22840-5785-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5785-5 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
VANILLA vanilla planifolia solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5754
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VANILLA (VANILLA) VANILLA 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5754-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5754-2 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
WHOLE WHEAT triticum aestivum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5756
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WHEAT (WHEAT) WHEAT 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5756-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5756-2 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
APRICOT prunus armeniaca solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5701
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
APRICOT (APRICOT) APRICOT 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:22840-5701-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5701-2 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
WHOLE GRAIN BARLEY hordeum vulgare solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5703
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BARLEY (BARLEY) BARLEY 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5703-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5703-2 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
NAVY BEAN phaseolus vulgaris solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5705
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
KIDNEY BEAN (KIDNEY BEAN) KIDNEY BEAN 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5705-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5705-2 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
STRING GREEN BEAN phaseolus vulgaris solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5706
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
STRING BEAN (STRING BEAN) STRING BEAN 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5706-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5706-2 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
CABBAGE brassica oleracea var. capitata solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5710
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CABBAGE (CABBAGE) CABBAGE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5710-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5710-2 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
CINNAMON cinnamomum verum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5717
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CINNAMON (CINNAMON) CINNAMON 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5717-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5717-2 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
COFFEE coffea arabica solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5718
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COFFEA ARABICA SEED, ROASTED (COFFEA ARABICA SEED, ROASTED) COFFEA ARABICA SEED, ROASTED 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5718-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5718-2 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
MUSHROOM agaricus campestris solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5730
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FIELD MUSHROOM (FIELD MUSHROOM) FIELD MUSHROOM 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:22840-5730-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5730-2 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
MUSTARD FOOD sinapis alba solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5731
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WHITE MUSTARD SEED (WHITE MUSTARD SEED) WHITE MUSTARD SEED 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:22840-5731-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5731-2 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
BANANA musa acuminata solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5702
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUSA ACUMINATA FRUIT (MUSA ACUMINATA FRUIT) MUSA ACUMINATA FRUIT 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:22840-5702-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5702-2 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
COCONUT cocos nucifera solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5784
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCONUT (COCONUT) COCONUT 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:22840-5784-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5784-5 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
CORN FOOD zea mays solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5719
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CORN (CORN) CORN 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:22840-5719-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5719-2 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
MALT hordeum vulgare solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5729
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BARLEY (BARLEY) BARLEY 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5729-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5729-2 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
BLACK PEPPER piper nigrum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5740
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BLACK PEPPER (BLACK PEPPER) BLACK PEPPER 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5740-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5740-2 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
LEMON citrus x limon solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5727
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LEMON (LEMON) LEMON 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:22840-5727-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5727-2 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
OAT FOOD avena sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5733
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OAT (OAT) OAT 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5733-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5733-2 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
ONION allium cepa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5735
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ONION (ONION) ONION 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5735-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5735-2 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
CUCUMBER cucumis sativus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5721
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CUCUMBER (CUCUMBER) CUCUMBER 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:22840-5721-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5721-2 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
BLUEBERRY vaccinium myrtilloides solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5707
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VELVETLEAF HUCKLEBERRY (VELVETLEAF HUCKLEBERRY) VELVETLEAF HUCKLEBERRY 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5707-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5707-2 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
GINGER zingiber officinale solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5723
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GINGER (GINGER) GINGER 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5723-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5723-2 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
WHITE SEEDLESS GRAPE vitis vinifera solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5724
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WINE GRAPE (WINE GRAPE) WINE GRAPE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5724-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5724-2 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
TOMATO solanum lycopersicum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5753
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TOMATO (TOMATO) TOMATO 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5753-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5753-2 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
GARLIC allium sativum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5722
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GARLIC (GARLIC) GARLIC 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5722-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5722-2 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
SOYBEAN FOOD glycine max solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5749
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SOYBEAN (SOYBEAN) SOYBEAN 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5749-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5749-2 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
SPINACH spinacia oleracea solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5750
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SPINACH (SPINACH) SPINACH 0.01 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5750-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5750-2 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
GREEN PEPPER piper nigrum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5741
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GREEN BELL PEPPER (GREEN BELL PEPPER) GREEN BELL PEPPER 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:22840-5741-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5741-2 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
PINEAPPLE ananas comosus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5742
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PINEAPPLE (PINEAPPLE) PINEAPPLE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5742-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5742-2 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
STRAWBERRY fragaria x ananassa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5752
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
STRAWBERRY (STRAWBERRY) STRAWBERRY 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5752-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5752-2 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
YELLOW SUMMER SQUASH cucurbita pepo var. ovifera solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5751
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CUCURBITA PEPO SUBSP. OVIFERA WHOLE (CUCURBITA PEPO SUBSP. OVIFERA WHOLE) CUCURBITA PEPO SUBSP. OVIFERA WHOLE 0.025 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5751-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5751-2 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
BRAZIL NUT bertholletia excelsa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5782
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BERTHOLLETIA EXCELSA WHOLE (BERTHOLLETIA EXCELSA WHOLE) BERTHOLLETIA EXCELSA WHOLE 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:22840-5782-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5782-5 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
CRANBERRY vaccinium macrocarpon solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5720
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CRANBERRY (CRANBERRY) CRANBERRY 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:22840-5720-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5720-2 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
GREEN OLIVE olea europaea solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5734
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GREEN OLIVE (GREEN OLIVE) GREEN OLIVE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5734-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5734-2 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
CHERRY prunus avium solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5715
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SWEET CHERRY (SWEET CHERRY) SWEET CHERRY 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5715-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5715-2 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
LIMA BEAN phaseolus lunatus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5704
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIMA BEAN (LIMA BEAN) LIMA BEAN 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5704-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5704-2 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
HOPS FOOD humulus lupulus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5726
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HOPS (HOPS) HOPS 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5726-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5726-2 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
NUTMEG myristica fragrans solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5732
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MYRISTICA FRAGRANS FRUIT (MYRISTICA FRAGRANS FRUIT) MYRISTICA FRAGRANS FRUIT 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5732-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5732-2 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
PECAN FOOD carya illinoinensis solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5787
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PECAN (PECAN) PECAN 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5787-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5787-2 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
SWEET POTATO ipomoea batatas solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5743
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SWEET POTATO (SWEET POTATO) SWEET POTATO 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5743-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5743-2 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
WHITE POTATO solanum tuberosum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5744
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POTATO (POTATO) POTATO 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5744-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5744-2 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
RED RASPBERRY rubus idaeus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5745
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RASPBERRY (RASPBERRY) RASPBERRY 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5745-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5745-2 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
ORANGE citrus x sinensis solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5736
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ORANGE (ORANGE) ORANGE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5736-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5736-2 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
BLACK WALNUT FOOD juglans nigra solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5788
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BLACK WALNUT (BLACK WALNUT) BLACK WALNUT 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5788-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5788-2 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
WATERMELON citrullus lanatus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5755
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WATERMELON (WATERMELON) WATERMELON 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5755-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5755-2 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
GRAPEFRUIT citrus x paradisi solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5725
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GRAPEFRUIT (GRAPEFRUIT) GRAPEFRUIT 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:22840-5725-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5725-2 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
PEACH prunus persica solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5738
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PEACH (PEACH) PEACH 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:22840-5738-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5738-2 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
PEANUT arachis hypogaea solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5786
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PEANUT (PEANUT) PEANUT 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5786-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5786-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5786-4 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
GREEN ENGLISH PEA pisum sativum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5737
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PISUM SATIVUM WHOLE (PISUM SATIVUM WHOLE) PISUM SATIVUM WHOLE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5737-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5737-2 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
PEAR pyrus communis solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5739
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PEAR (PEAR) PEAR 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:22840-5739-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5739-2 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
BEEF bos taurus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5757
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BEEF (BEEF) BEEF 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:22840-5757-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5757-5 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
CHICKEN MEAT gallus gallus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5760
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHICKEN (CHICKEN) CHICKEN 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:22840-5760-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5760-5 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
CHICKEN EGG WHITE gallus gallus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5761
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EGG WHITE (EGG WHITE) EGG WHITE 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5761-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5761-2 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
CHICKEN EGG YOLK gallus gallus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5763
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EGG YOLK (EGG YOLK) EGG YOLK 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:22840-5763-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5763-2 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
CHICKEN EGG WHOLE gallus gallus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5762
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EGG (EGG) EGG 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:22840-5762-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5762-2 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
LAMB ovis aries solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5758
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LAMB (LAMB) LAMB 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:22840-5758-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5758-5 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
PORK sus scrofa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5759
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PORK (PORK) PORK 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:22840-5759-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5759-2 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
TURKEY MEAT meleagris gallopavo solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5764
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TURKEY (TURKEY) TURKEY 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:22840-5764-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5764-5 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
COW MILK bos taurus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5765
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SKIM MILK (SKIM MILK) SKIM MILK 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:22840-5765-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5765-2 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
BLACK BASS centropristis striata solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5766
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BLACK SEA BASS (BLACK SEA BASS) BLACK SEA BASS 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:22840-5766-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5766-5 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
CATFISH ictalurus punctatus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5767
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHANNEL CATFISH (CHANNEL CATFISH) CHANNEL CATFISH 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:22840-5767-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5767-2 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
CLAM mercenaria mercenaria solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5768
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NORTHERN QUAHOG (NORTHERN QUAHOG) NORTHERN QUAHOG 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:22840-5768-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5768-2 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
ATLANTIC COD gadus morhua solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5769
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ATLANTIC COD (ATLANTIC COD) ATLANTIC COD 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:22840-5769-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5769-5 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
CRAB callinectes sapidus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5770
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BLUE CRAB (BLUE CRAB) BLUE CRAB 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:22840-5770-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5770-5 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
FISH MIX gadus morhua, paralichthys lethostigma, hippoglossus hippoglossus, scomber scombrus and thunnus albacares solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9700
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SOUTHERN FLOUNDER (SOUTHERN FLOUNDER) SOUTHERN FLOUNDER 0.01 g in 1 mL
ATLANTIC MACKEREL (ATLANTIC MACKEREL) ATLANTIC MACKEREL 0.01 g in 1 mL
YELLOWFIN TUNA (YELLOWFIN TUNA) YELLOWFIN TUNA 0.01 g in 1 mL
ATLANTIC COD (ATLANTIC COD) ATLANTIC COD 0.01 g in 1 mL
ATLANTIC HALIBUT (ATLANTIC HALIBUT) ATLANTIC HALIBUT 0.01 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9700-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-9700-2 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
SHELLFISH MIX mercenaria mercenaria, callinectes sapidus, crassostrea virginica, placopecten magellanicus and farfantepenaeus aztecus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-9701
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BLUE CRAB (BLUE CRAB) BLUE CRAB 0.01 g in 1 mL
NORTHERN QUAHOG (NORTHERN QUAHOG) NORTHERN QUAHOG 0.01 g in 1 mL
EASTERN OYSTER (EASTERN OYSTER) EASTERN OYSTER 0.01 g in 1 mL
SEA SCALLOP (SEA SCALLOP) SEA SCALLOP 0.01 g in 1 mL
NORTHERN BROWN SHRIMP (NORTHERN BROWN SHRIMP) NORTHERN BROWN SHRIMP 0.01 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-9701-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-9701-5 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
FLOUNDER paralichthys lethostigma solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5771
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SOUTHERN FLOUNDER (SOUTHERN FLOUNDER) SOUTHERN FLOUNDER 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5771-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5771-2 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
MAINE LOBSTER homarus americanus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5772
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AMERICAN LOBSTER (AMERICAN LOBSTER) AMERICAN LOBSTER 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:22840-5772-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5772-5 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
MACKEREL scomber scombrus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5773
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ATLANTIC MACKEREL (ATLANTIC MACKEREL) ATLANTIC MACKEREL 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:22840-5773-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5773-5 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
OYSTER crassostrea virginica solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5774
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EASTERN OYSTER (EASTERN OYSTER) EASTERN OYSTER 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:22840-5774-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5774-5 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
OCEAN PERCH sebastes alutus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5775
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PACIFIC OCEAN PERCH (PACIFIC OCEAN PERCH) PACIFIC OCEAN PERCH 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:22840-5775-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5775-5 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
SALMON salmo salar solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5776
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ATLANTIC SALMON (ATLANTIC SALMON) ATLANTIC SALMON 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:22840-5776-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5776-5 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
SCALLOPS placopecten magellanicus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5777
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SEA SCALLOP (SEA SCALLOP) SEA SCALLOP 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:22840-5777-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5777-5 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
SHRIMP farfantepenaeus aztecus solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5778
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NORTHERN BROWN SHRIMP (NORTHERN BROWN SHRIMP) NORTHERN BROWN SHRIMP 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:22840-5778-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5778-5 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
LAKE TROUT oncorhynchus mykiss solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5779
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RAINBOW TROUT (RAINBOW TROUT) RAINBOW TROUT 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5779-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5779-2 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
TUNA thunnus albacares solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5780
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
YELLOWFIN TUNA (YELLOWFIN TUNA) YELLOWFIN TUNA 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:22840-5780-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5780-2 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
ALMOND FOOD prunus dulcis solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5781
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALMOND (ALMOND) ALMOND 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:22840-5781-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5781-5 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
APPLE malus pumila solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5700
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
APPLE (APPLE) APPLE 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:22840-5700-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5700-2 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
ENGLISH WALNUT juglans regia solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5789
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ENGLISH WALNUT (ENGLISH WALNUT) ENGLISH WALNUT 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
PHENOL
SODIUM BICARBONATE
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5789-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5789-2 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
Labeler — Greer Laboratories, Inc. (024671414)
Registrant — Greer Laboratories, Inc. (024671414)
Establishment
Name Address ID/FEI Operations
Greer Laboratories, Inc. 024671414 manufacture (22840-1175), manufacture (22840-1176), manufacture (22840-1537), manufacture (22840-1538), manufacture (22840-5100), manufacture (22840-5101), manufacture (22840-5102), manufacture (22840-5103), manufacture (22840-5104), manufacture (22840-5105), manufacture (22840-5106), manufacture (22840-5107), manufacture (22840-5108), manufacture (22840-5109), manufacture (22840-5110), manufacture (22840-5111), manufacture (22840-5112), manufacture (22840-5113), manufacture (22840-5114), manufacture (22840-5115), manufacture (22840-5517), manufacture (22840-9100), manufacture (22840-9101), manufacture (22840-9102), manufacture (22840-9103), manufacture (22840-9104), manufacture (22840-9105), manufacture (22840-9107), manufacture (22840-1174), manufacture (22840-1100), manufacture (22840-1101), manufacture (22840-1102), manufacture (22840-1103), manufacture (22840-1105), manufacture (22840-1106), manufacture (22840-1107), manufacture (22840-1108), manufacture (22840-1110), manufacture (22840-1111), manufacture (22840-1112), manufacture (22840-1113), manufacture (22840-1116), manufacture (22840-1117), manufacture (22840-1118), manufacture (22840-1119), manufacture (22840-1121), manufacture (22840-1122), manufacture (22840-1123), manufacture (22840-1125), manufacture (22840-1126), manufacture (22840-1127), manufacture (22840-1128), manufacture (22840-1129), manufacture (22840-1130), manufacture (22840-1131), manufacture (22840-1133), manufacture (22840-1134), manufacture (22840-1135), manufacture (22840-1136), manufacture (22840-1138), manufacture (22840-1139), manufacture (22840-1140), manufacture (22840-1141), manufacture (22840-1142), manufacture (22840-1144), manufacture (22840-1145), manufacture (22840-1146), manufacture (22840-1147), manufacture (22840-1149), manufacture (22840-1150), manufacture (22840-1151), manufacture (22840-1153), manufacture (22840-1154), manufacture (22840-1155), manufacture (22840-1157), manufacture (22840-1159), manufacture (22840-1160), manufacture (22840-1162), manufacture (22840-1163), manufacture (22840-1164), manufacture (22840-1167), manufacture (22840-1168), manufacture (22840-1169), manufacture (22840-1170), manufacture (22840-1171), manufacture (22840-1173)

Revised: 11/2019 Greer Laboratories, Inc.

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