Alfalfa: 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

1509-1_Alfalfa_1000-wv
(click image for full-size original)

5520-5_Cultivated Corn_20-wv
(click image for full-size original)
1567-2_Cultivated Wheat_20000-pnu
(click image for full-size original)
1578-4_Common Cultivated Oats_10-wv
(click image for full-size original)
ALFALFA medicago sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1507
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MEDICAGO SATIVA POLLEN (MEDICAGO SATIVA POLLEN) MEDICAGO SATIVA POLLEN 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:22840-1507-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1507-4 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
SUGAR BEET POLLEN beta vulgaris solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1517
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BETA VULGARIS POLLEN (BETA VULGARIS POLLEN) BETA VULGARIS POLLEN 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:22840-1517-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1517-4 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
CULTIVATED CORN zea mays solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5520
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ZEA MAYS POLLEN (ZEA MAYS POLLEN) ZEA MAYS POLLEN 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:22840-5520-5 5 mL in 1 BOTTLE, DROPPER None
2 NDC:22840-5520-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5520-4 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
CULTIVATED CORN zea mays solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1574
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ZEA MAYS POLLEN (ZEA MAYS POLLEN) ZEA MAYS POLLEN 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:22840-1574-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1574-4 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
MUSTARD brassica spp. solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1512
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BRASSICA RAPA POLLEN (BRASSICA RAPA POLLEN) BRASSICA RAPA POLLEN 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:22840-1512-1 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
COMMON CULTIVATED OATS avena sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1578
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AVENA SATIVA POLLEN (AVENA SATIVA POLLEN) AVENA SATIVA POLLEN 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:22840-1578-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1578-4 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
RED CLOVER trifolium pratense solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1514
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRIFOLIUM PRATENSE POLLEN (TRIFOLIUM PRATENSE POLLEN) TRIFOLIUM PRATENSE POLLEN 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:22840-1514-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1514-4 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
CULTIVATED RYE secale cereale solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1585
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SECALE CEREALE POLLEN (SECALE CEREALE POLLEN) SECALE CEREALE POLLEN 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:22840-1585-1 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
CULTIVATED RYE secale cereale solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5522
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SECALE CEREALE POLLEN (SECALE CEREALE POLLEN) SECALE CEREALE POLLEN 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:22840-5522-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5522-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5522-5 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
CULTIVATED WHEAT triticum aestivum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1567
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRITICUM AESTIVUM POLLEN (TRITICUM AESTIVUM POLLEN) TRITICUM AESTIVUM POLLEN 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1567-2 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
CULTIVATED WHEAT triticum aestivum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1568
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRITICUM AESTIVUM POLLEN (TRITICUM AESTIVUM POLLEN) TRITICUM AESTIVUM POLLEN 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:22840-1568-2 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
CULTIVATED WHEAT triticum aestivum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1590
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRITICUM AESTIVUM POLLEN (TRITICUM AESTIVUM POLLEN) TRITICUM AESTIVUM POLLEN 1000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1590-1 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
CULTIVATED WHEAT triticum aestivum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1588
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRITICUM AESTIVUM POLLEN (TRITICUM AESTIVUM POLLEN) TRITICUM AESTIVUM POLLEN 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1588-2 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
CULTIVATED WHEAT triticum aestivum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5523
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRITICUM AESTIVUM POLLEN (TRITICUM AESTIVUM POLLEN) TRITICUM AESTIVUM POLLEN 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:22840-5523-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5523-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5523-5 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
MUSTARD brassica spp. solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1513
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BRASSICA RAPA POLLEN (BRASSICA RAPA POLLEN) BRASSICA RAPA POLLEN 1000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1513-1 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
RED CLOVER trifolium pratense solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1565
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRIFOLIUM PRATENSE POLLEN (TRIFOLIUM PRATENSE POLLEN) TRIFOLIUM PRATENSE POLLEN 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1565-2 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 CLOVER trifolium pratense solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1515
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRIFOLIUM PRATENSE POLLEN (TRIFOLIUM PRATENSE POLLEN) TRIFOLIUM PRATENSE POLLEN 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:22840-1515-1 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
RED CLOVER trifolium pratense solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5506
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRIFOLIUM PRATENSE POLLEN (TRIFOLIUM PRATENSE POLLEN) TRIFOLIUM PRATENSE POLLEN 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:22840-5506-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5506-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5506-5 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
CULTIVATED WHEAT triticum aestivum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1589
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRITICUM AESTIVUM POLLEN (TRITICUM AESTIVUM POLLEN) TRITICUM AESTIVUM POLLEN 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:22840-1589-1 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
CULTIVATED RYE secale cereale solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1584
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SECALE CEREALE POLLEN (SECALE CEREALE POLLEN) SECALE CEREALE POLLEN 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:22840-1584-4 50 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1584-2 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
CULTIVATED WHEAT triticum aestivum solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1587
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRITICUM AESTIVUM POLLEN (TRITICUM AESTIVUM POLLEN) TRITICUM AESTIVUM POLLEN 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:22840-1587-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1587-4 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
CULTIVATED CORN zea mays solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1562
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ZEA MAYS POLLEN (ZEA MAYS POLLEN) ZEA MAYS POLLEN 0.05 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1562-2 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
CULTIVATED CORN zea mays solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1577
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ZEA MAYS POLLEN (ZEA MAYS POLLEN) ZEA MAYS POLLEN 1000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1577-1 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
COMMON CULTIVATED OATS avena sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1582
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AVENA SATIVA POLLEN (AVENA SATIVA POLLEN) AVENA SATIVA POLLEN 1000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1582-1 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
SUGAR BEET POLLEN beta vulgaris solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5507
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BETA VULGARIS POLLEN (BETA VULGARIS POLLEN) BETA VULGARIS POLLEN 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:22840-5507-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5507-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5507-5 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
COMMON CULTIVATED OATS avena sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1579
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AVENA SATIVA POLLEN (AVENA SATIVA POLLEN) AVENA SATIVA POLLEN 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1579-2 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 brassica spp. solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5505
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BRASSICA RAPA POLLEN (BRASSICA RAPA POLLEN) BRASSICA RAPA POLLEN 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:22840-5505-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5505-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5505-5 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
CULTIVATED RYE secale cereale solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1586
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SECALE CEREALE POLLEN (SECALE CEREALE POLLEN) SECALE CEREALE POLLEN 1000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1586-1 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
CULTIVATED CORN zea mays solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1576
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ZEA MAYS POLLEN (ZEA MAYS POLLEN) ZEA MAYS POLLEN 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:22840-1576-1 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
CULTIVATED CORN zea mays solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1575
Route of Administration SUBCUTANEOUS, INTRADERMAL, PERCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ZEA MAYS POLLEN (ZEA MAYS POLLEN) ZEA MAYS POLLEN 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1575-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1575-4 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
CULTIVATED CORN zea mays solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1563
Route of Administration PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ZEA MAYS POLLEN (ZEA MAYS POLLEN) ZEA MAYS POLLEN 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1563-4 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
COMMON CULTIVATED OATS avena sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5521
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AVENA SATIVA POLLEN (AVENA SATIVA POLLEN) AVENA SATIVA POLLEN 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:22840-5521-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5521-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5521-5 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
CULTIVATED RYE secale cereale solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1566
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SECALE CEREALE POLLEN (SECALE CEREALE POLLEN) SECALE CEREALE POLLEN 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1566-2 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
CULTIVATED RYE secale cereale solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1583
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SECALE CEREALE POLLEN (SECALE CEREALE POLLEN) SECALE CEREALE POLLEN 40000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1583-2 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
SUGAR BEET POLLEN beta vulgaris solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1516
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BETA VULGARIS POLLEN (BETA VULGARIS POLLEN) BETA VULGARIS POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1516-2 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
SUGAR BEET POLLEN beta vulgaris solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1518
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BETA VULGARIS POLLEN (BETA VULGARIS POLLEN) BETA VULGARIS POLLEN 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:22840-1518-1 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
ALFALFA medicago sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1508
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MEDICAGO SATIVA POLLEN (MEDICAGO SATIVA POLLEN) MEDICAGO SATIVA POLLEN 1000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1508-1 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
ALFALFA medicago sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1561
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MEDICAGO SATIVA POLLEN (MEDICAGO SATIVA POLLEN) MEDICAGO SATIVA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1561-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1561-4 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
ALFALFA medicago sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1509
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MEDICAGO SATIVA POLLEN (MEDICAGO SATIVA POLLEN) MEDICAGO SATIVA POLLEN 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:22840-1509-1 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
ALFALFA medicago sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-5503
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MEDICAGO SATIVA POLLEN (MEDICAGO SATIVA POLLEN) MEDICAGO SATIVA POLLEN 0.02 g in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
GLYCERIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-5503-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-5503-4 50 mL in 1 VIAL, MULTI-DOSE None
3 NDC:22840-5503-5 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
COMMON CULTIVATED OATS avena sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1580
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AVENA SATIVA POLLEN (AVENA SATIVA POLLEN) AVENA SATIVA POLLEN 20000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
PHENOL
SODIUM CHLORIDE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:22840-1580-2 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
COMMON CULTIVATED OATS avena sativa solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1581
Route of Administration PERCUTANEOUS, INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AVENA SATIVA POLLEN (AVENA SATIVA POLLEN) AVENA SATIVA POLLEN 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:22840-1581-1 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
MUSTARD brassica spp. solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1511
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BRASSICA RAPA POLLEN (BRASSICA RAPA POLLEN) BRASSICA RAPA POLLEN 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:22840-1511-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1511-4 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
MUSTARD brassica spp. solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC Item Code (Source) NDC:22840-1564
Route of Administration INTRADERMAL, PERCUTANEOUS, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BRASSICA RAPA POLLEN (BRASSICA RAPA POLLEN) BRASSICA RAPA POLLEN 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:22840-1564-2 10 mL in 1 VIAL, MULTI-DOSE None
2 NDC:22840-1564-4 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
Labeler — Greer Laboratories, Inc. (024671414)
Registrant — Greer Laboratories, Inc. (024671414)
Establishment
Name Address ID/FEI Operations
Greer Laboratories, Inc. 024671414 manufacture (22840-1164), manufacture (22840-1167), manufacture (22840-1168), manufacture (22840-1169), manufacture (22840-1170), manufacture (22840-1171), manufacture (22840-1173), manufacture (22840-1174), 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 (22840-1144), 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 (22840-1145), 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)

Revised: 11/2019 Greer Laboratories, Inc.

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