Acacia (Page 4 of 4)

HOW SUPPLIED

Allergenic extracts are supplied with units listed as: Weight/volume (W/V), Protein Nitrogen Units (PNU/ml), Allergy Units (AU/ml) or Bioequivalent Allergy Units (BAU/ml).

Sizes:

Diagnostic Scratch: 5 ml dropper application vials

Diagnostic Intradermal: 5 ml or 10 ml vials.

Therapeutic Allergens: 5 ml, 10 ml, 50 ml multiple dose vials.

STORAGE

The expiration date of allergen extracts is listed on the container label. Store extracts upon arrival at 2° to 8°C and keep them in this range during office use.

WARRANTY: We warrant that this product was prepared and tested according to the standards of the FDA and is true to label. Because of biological differences in individuals and because allergenic extracts are manufactured to be potent and because we have no control over the conditions of use, we cannot and do not warrant either a good effect or against an ill effect following use.

REFERENCES

1 Jacobs, Robert L., Geoffrey W.Rake,Jr., et.al. Potentiated Anaphylaxis in Patients with Drug-induced Beta-adrenergic Blockade. J.Allergy & Clin. Immunol., 68(2): 125-127. August 1981.

2 Ishizaka,K.: Cellular Events in the IgE Antibody Response. Adv. in Immuno. 23:50-75, 1976.

3. Lockey, R.F., Bukantz, S.C., Allergen Immunotherapy. New York,NY: Marcel Dekker Inc., 1991.

4. Reid,M.J., Lockey,R.F., Turkeltaub,P.C., Platts-Mills,T.A.E., Survey of fatalities from skin testing and immunotherapy 1985-1989. Journal of Allergy Clin. Immunol. 92 (1): 6-15, July 1993.

5. Murray, A.B., Ferguson, A., Morrison, B., The frequency and severity of cat allergy vs dog allergy in atopic children. J. Allergy Clin. Immunolo: 72, 145-9, 1983.

6. Lockey, R.F., Bukantz, S.C., Allergen Immunotherapy. New York,NY: Marcel Dekker Inc., 1991.

CONTAINER LABELING

5 mL Stock Intradermal
(click image for full-size original)
5 mL Stock Scratch
(click image for full-size original)
Stock Small Label
(click image for full-size original)
Stock Large Label
(click image for full-size original)
ACACIA acacia injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2445
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACACIA BAILEYANA POLLEN (ACACIA BAILEYANA POLLEN) ACACIA BAILEYANA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2445-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2445-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2445-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2445-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
RED ALDER red alder injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2453
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALNUS RUBRA POLLEN (ALNUS RUBRA POLLEN) ALNUS RUBRA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2453-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2453-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2453-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2453-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
TAG ALDER tag alder injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2461
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALNUS INCANA SUBSP. RUGOSA POLLEN (ALNUS INCANA SUBSP. RUGOSA POLLEN) ALNUS INCANA SUBSP. RUGOSA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2461-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2461-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2461-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2461-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WHITE ALDER white alder injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2469
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALNUS RHOMBIFOLIA POLLEN (ALNUS RHOMBIFOLIA POLLEN) ALNUS RHOMBIFOLIA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
WATER
SODIUM BICARBONATE
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2469-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2469-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2469-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2469-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
ARIZONA ASH arizona ash injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2477
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FRAXINUS VELUTINA POLLEN (FRAXINUS VELUTINA POLLEN) FRAXINUS VELUTINA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2477-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2477-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2477-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2477-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
OREGON ASH oregon ash injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2485
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FRAXINUS LATIFOLIA POLLEN (FRAXINUS LATIFOLIA POLLEN) FRAXINUS LATIFOLIA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2485-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2485-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2485-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2485-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WHITE ASH white ash injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2493
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FRAXINUS AMERICANA POLLEN (FRAXINUS AMERICANA POLLEN) FRAXINUS AMERICANA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2493-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2493-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2493-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2493-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
ASPEN aspen injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2501
Route of Administration SUBCUTANEOUS, INTRADERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POPULUS TREMULOIDES POLLEN (POPULUS TREMULOIDES POLLEN) POPULUS TREMULOIDES POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2501-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2501-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2501-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2501-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
BAYBERRY bayberry injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2509
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MORELLA CERIFERA POLLEN (MORELLA CERIFERA POLLEN) MORELLA CERIFERA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2509-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2509-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2509-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2509-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
AMERICAN BEECH american beech injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2517
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FAGUS GRANDIFOLIA POLLEN (FAGUS GRANDIFOLIA POLLEN) FAGUS GRANDIFOLIA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2517-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2517-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2517-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2517-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
BEEFWOOD/AUSTRALIAN PINE beefwood/australian pine injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2525
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CASUARINA EQUISETIFOLIA POLLEN (CASUARINA EQUISETIFOLIA POLLEN) CASUARINA EQUISETIFOLIA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2525-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2525-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2525-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2525-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
BIRCH birch injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2533
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BETULA NIGRA POLLEN (BETULA NIGRA POLLEN) BETULA NIGRA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2533-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2533-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2533-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2533-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
BLACK BIRCH black birch injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2541
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BETULA LENTA POLLEN (BETULA LENTA POLLEN) BETULA LENTA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2541-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2541-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2541-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2541-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WHITE BIRCH white birch injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2549
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BETULA POPULIFOLIA POLLEN (BETULA POPULIFOLIA POLLEN) BETULA POPULIFOLIA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2549-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2549-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2549-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2549-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
BOX ELDER box elder injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2557
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACER NEGUNDO POLLEN (ACER NEGUNDO POLLEN) ACER NEGUNDO POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2557-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2557-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2557-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2557-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
MOUNTAIN CEDAR mountain cedar injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2565
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
JUNIPERUS ASHEI POLLEN (JUNIPERUS ASHEI POLLEN) JUNIPERUS ASHEI POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2565-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2565-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2565-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2565-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
RED CEDAR red cedar injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2573
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
JUNIPERUS VIRGINIANA POLLEN (JUNIPERUS VIRGINIANA POLLEN) JUNIPERUS VIRGINIANA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2573-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2573-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2573-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2573-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
SALT CEDAR salt cedar injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2581
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TAMARIX GALLICA POLLEN (TAMARIX GALLICA POLLEN) TAMARIX GALLICA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM BICARBONATE
SODIUM CHLORIDE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2581-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2581-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2581-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2581-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
EASTERN COTTONWOOD eastern cottonwood injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2589
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POPULUS DELTOIDES POLLEN (POPULUS DELTOIDES POLLEN) POPULUS DELTOIDES POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2589-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2589-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2589-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2589-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
FREMONT COTTONWOOD fremont cottonwood injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2597
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POPULUS FREMONTII POLLEN (POPULUS FREMONTII POLLEN) POPULUS FREMONTII POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2597-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2597-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2597-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2597-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WEST COTTONWOOD west cottonwood injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2605
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN (POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN) POPULUS DELTOIDES SUBSP. MONILIFERA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2605-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2605-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2605-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2605-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
ARIZONA CYPRESS arizona cypress injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2613
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CUPRESSUS ARIZONICA POLLEN (CUPRESSUS ARIZONICA POLLEN) CUPRESSUS ARIZONICA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2613-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2613-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2613-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2613-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
BALD CYPRESS bald cypress injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2621
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TAXODIUM DISTICHUM POLLEN (TAXODIUM DISTICHUM POLLEN) TAXODIUM DISTICHUM POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2621-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2621-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2621-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2621-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
AMERICAN ELM american elm injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2629
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ULMUS AMERICANA POLLEN (ULMUS AMERICANA POLLEN) ULMUS AMERICANA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2629-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2629-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2629-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2629-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
CEDAR ELM cedar elm injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2637
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ULMUS CRASSIFOLIA POLLEN (ULMUS CRASSIFOLIA POLLEN) ULMUS CRASSIFOLIA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2637-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2637-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2637-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2637-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
CHINESE ELM chinese elm injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2645
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ULMUS PUMILA POLLEN (ULMUS PUMILA POLLEN) ULMUS PUMILA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2645-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2645-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2645-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2645-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
EUCALYPTUS eucalyptus injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2653
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EUCALYPTUS GLOBULUS POLLEN (EUCALYPTUS GLOBULUS POLLEN) EUCALYPTUS GLOBULUS POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2653-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2653-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2653-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2653-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
HAZELNUT hazelnut injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2661
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CORYLUS AMERICANA POLLEN (CORYLUS AMERICANA POLLEN) CORYLUS AMERICANA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2661-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2661-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2661-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2661-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
SHAGBARK HICKORY shagbark hickory injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2669
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CARYA OVATA POLLEN (CARYA OVATA POLLEN) CARYA OVATA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2669-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2669-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2669-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2669-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WHITE HICKORY white hickory injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2677
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CARYA ALBA POLLEN (CARYA ALBA POLLEN) CARYA ALBA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2677-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2677-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2677-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2677-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
ONE SEED JUNIPER one seed juniper injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2685
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
JUNIPERUS MONOSPERMA POLLEN (JUNIPERUS MONOSPERMA POLLEN) JUNIPERUS MONOSPERMA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2685-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2685-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2685-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2685-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
PINCHOT JUNIPER pinchot juniper injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2693
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
JUNIPERUS PINCHOTII POLLEN (JUNIPERUS PINCHOTII POLLEN) JUNIPERUS PINCHOTII POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2693-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2693-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2693-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2693-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
ROCKY MOUNTAIN JUNIPER rocky mountain juniper injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2701
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
JUNIPERUS SCOPULORUM POLLEN (JUNIPERUS SCOPULORUM POLLEN) JUNIPERUS SCOPULORUM POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2701-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2701-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2701-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2701-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
UTAH JUNIPER utah juniper injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2709
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
JUNIPERUS OSTEOSPERMA POLLEN (JUNIPERUS OSTEOSPERMA POLLEN) JUNIPERUS OSTEOSPERMA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2709-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2709-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2709-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2709-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WESTERN JUNIPER western juniper injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2717
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
JUNIPERUS OCCIDENTALIS POLLEN (JUNIPERUS OCCIDENTALIS POLLEN) JUNIPERUS OCCIDENTALIS POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2717-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2717-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2717-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2717-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
LINDEN linden injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2725
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TILIA AMERICANA POLLEN (TILIA AMERICANA POLLEN) TILIA AMERICANA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2725-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2725-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2725-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2725-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
BLACK LOCUST black locust injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2733
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ROBINIA PSEUDOACACIA POLLEN (ROBINIA PSEUDOACACIA POLLEN) ROBINIA PSEUDOACACIA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2733-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2733-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2733-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2733-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
MANGO BLOSSOM mango blossom injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2741
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MANGIFERA INDICA POLLEN (MANGIFERA INDICA POLLEN) MANGIFERA INDICA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2741-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2741-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2741-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2741-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
COAST MAPLE coast maple injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2749
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACER MACROPHYLLUM POLLEN (ACER MACROPHYLLUM POLLEN) ACER MACROPHYLLUM POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2749-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2749-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2749-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2749-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
RED MAPLE red maple injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2757
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACER RUBRUM POLLEN (ACER RUBRUM POLLEN) ACER RUBRUM POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2757-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2757-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2757-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2757-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
SILVER MAPLE silver maple injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2765
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACER SACCHARINUM POLLEN (ACER SACCHARINUM POLLEN) ACER SACCHARINUM POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2765-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2765-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2765-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2765-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
SUGAR MAPLE sugar maple injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2773
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACER SACCHARUM POLLEN (ACER SACCHARUM POLLEN) ACER SACCHARUM POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2773-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2773-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2773-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2773-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
MELALEUCA POLLEN melaleuca pollen injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2781
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MELALEUCA QUINQUENERVIA POLLEN (MELALEUCA QUINQUENERVIA POLLEN) MELALEUCA QUINQUENERVIA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2781-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2781-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2781-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2781-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
MESQUITE mesquite injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2789
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PROSOPIS JULIFLORA POLLEN (PROSOPIS JULIFLORA POLLEN) PROSOPIS JULIFLORA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2789-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2789-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2789-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2789-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WHITE MULBERRY white mulberry injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2797
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MORUS ALBA POLLEN (MORUS ALBA POLLEN) MORUS ALBA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2797-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2797-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2797-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2797-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
RED MULBERRY red mulberry injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2805
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MORUS RUBRA POLLEN (MORUS RUBRA POLLEN) MORUS RUBRA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2805-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2805-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2805-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2805-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
MULBERRY mulberry injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2813
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BROUSSONETIA PAPYRIFERA POLLEN (BROUSSONETIA PAPYRIFERA POLLEN) BROUSSONETIA PAPYRIFERA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2813-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2813-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2813-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2813-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
BLACK OAK black oak injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2821
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS VELUTINA POLLEN (QUERCUS VELUTINA POLLEN) QUERCUS VELUTINA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2821-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2821-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2821-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2821-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
BURR OAK burr oak injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2829
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS MACROCARPA POLLEN (QUERCUS MACROCARPA POLLEN) QUERCUS MACROCARPA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2829-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2829-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2829-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2829-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
CALIFORNIA BLACK OAK california black oak injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2837
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS KELLOGGII POLLEN (QUERCUS KELLOGGII POLLEN) QUERCUS KELLOGGII POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2837-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2837-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2837-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2837-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
CALIFORNIA LIVE OAK california live oak injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2845
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS AGRIFOLIA POLLEN (QUERCUS AGRIFOLIA POLLEN) QUERCUS AGRIFOLIA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2845-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2845-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2845-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2845-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
GAMBIL OAK gambil oak injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2853
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS GAMBELII POLLEN (QUERCUS GAMBELII POLLEN) QUERCUS GAMBELII POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2853-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2853-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2853-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2853-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
RED OAK red oak injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2861
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS RUBRA POLLEN (QUERCUS RUBRA POLLEN) QUERCUS RUBRA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2861-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2861-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2861-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2861-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
CALIFORNIA VALLEY WHITE OAK california valley white oak injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2869
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS LOBATA POLLEN (QUERCUS LOBATA POLLEN) QUERCUS LOBATA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2869-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2869-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2869-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2869-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
VIRGINIA LIVE OAK virginia live oak injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2877
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS VIRGINIANA POLLEN (QUERCUS VIRGINIANA POLLEN) QUERCUS VIRGINIANA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2877-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2877-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2877-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2877-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WATER OAK water oak injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2885
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS NIGRA POLLEN (QUERCUS NIGRA POLLEN) QUERCUS NIGRA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2885-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2885-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2885-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2885-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WHITE OAK white oak injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2893
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS ALBA POLLEN (QUERCUS ALBA POLLEN) QUERCUS ALBA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2893-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2893-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2893-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2893-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
OLIVE POLLEN olive pollen injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2901
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OLEA EUROPAEA POLLEN (OLEA EUROPAEA POLLEN) OLEA EUROPAEA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2901-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2901-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2901-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2901-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
ORANGE POLLEN orange pollen injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2909
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CITRUS SINENSIS POLLEN (CITRUS SINENSIS POLLEN) CITRUS SINENSIS POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2909-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2909-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2909-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2909-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
QUEEN PALM queen palm injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2917
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SYAGRUS ROMANZOFFIANA POLLEN (SYAGRUS ROMANZOFFIANA POLLEN) SYAGRUS ROMANZOFFIANA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2917-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2917-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2917-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2917-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
PECAN POLLEN pecan pollen injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2925
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CARYA ILLINOINENSIS POLLEN (CARYA ILLINOINENSIS POLLEN) CARYA ILLINOINENSIS POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2925-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2925-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2925-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2925-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
PEPPER TREE POLLEN pepper tree pollen injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2933
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SCHINUS MOLLE POLLEN (SCHINUS MOLLE POLLEN) SCHINUS MOLLE POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2933-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2933-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2933-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2933-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 12/04/2009
LOBLOLLY PINE loblolly pine injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2941
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PINUS TAEDA POLLEN (PINUS TAEDA POLLEN) PINUS TAEDA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
PHENOL
SODIUM CHLORIDE
SODIUM BICARBONATE
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2941-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2941-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2941-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2941-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
LONGLEAF PINE longleaf pine injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2949
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PINUS PALUSTRIS POLLEN (PINUS PALUSTRIS POLLEN) PINUS PALUSTRIS POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2949-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2949-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2949-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2949-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
PONDEROSA PINE ponderosa pine injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2957
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PINUS PONDEROSA POLLEN (PINUS PONDEROSA POLLEN) PINUS PONDEROSA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2957-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2957-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2957-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2957-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
SLASH PINE slash pine injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2965
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PINUS ELLIOTTII POLLEN (PINUS ELLIOTTII POLLEN) PINUS ELLIOTTII POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2965-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2965-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2965-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2965-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
SCRUB PINE scrub pine injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2973
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PINUS VIRGINIANA POLLEN (PINUS VIRGINIANA POLLEN) PINUS VIRGINIANA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2973-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2973-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2973-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2973-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WHITE PINE white pine injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2981
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PINUS STROBUS POLLEN (PINUS STROBUS POLLEN) PINUS STROBUS POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2981-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2981-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2981-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2981-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WESTERN WHITE PINE western white pine injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2989
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PINUS MONTICOLA POLLEN (PINUS MONTICOLA POLLEN) PINUS MONTICOLA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2989-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2989-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2989-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2989-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
YELLOW PINE yellow pine injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-2997
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PINUS ECHINATA POLLEN (PINUS ECHINATA POLLEN) PINUS ECHINATA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-2997-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-2997-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-2997-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-2997-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
LOMBARDY POPLAR lombardy poplar injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3005
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POPULUS NIGRA POLLEN (POPULUS NIGRA POLLEN) POPULUS NIGRA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3005-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3005-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3005-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3005-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WHITE POPLAR white poplar injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3013
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POPULUS ALBA POLLEN (POPULUS ALBA POLLEN) POPULUS ALBA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3013-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3013-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3013-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3013-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
PRIVET privet injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3021
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIGUSTRUM VULGARE POLLEN (LIGUSTRUM VULGARE POLLEN) LIGUSTRUM VULGARE POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3021-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3021-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3021-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3021-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
RUSSIAN OLIVE russian olive injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3029
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ELAEAGNUS ANGUSTIFOLIA POLLEN (ELAEAGNUS ANGUSTIFOLIA POLLEN) ELAEAGNUS ANGUSTIFOLIA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3029-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3029-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3029-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3029-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
SWEET GUM sweet gum injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3037
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIQUIDAMBAR STYRACIFLUA POLLEN (LIQUIDAMBAR STYRACIFLUA POLLEN) LIQUIDAMBAR STYRACIFLUA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3037-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3037-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3037-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3037-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
EAST SYCAMORE east sycamore injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3045
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PLATANUS OCCIDENTALIS POLLEN (PLATANUS OCCIDENTALIS POLLEN) PLATANUS OCCIDENTALIS POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3045-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3045-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3045-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3045-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
WEST SYCAMORE west sycamore injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3053
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PLATANUS RACEMOSA POLLEN (PLATANUS RACEMOSA POLLEN) PLATANUS RACEMOSA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3053-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3053-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3053-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3053-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
BLACK WALNUT black walnut injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3061
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
JUGLANS NIGRA POLLEN (JUGLANS NIGRA POLLEN) JUGLANS NIGRA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3061-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3061-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3061-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3061-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
CALIFORNIA BLACK WALNUT california black walnut injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3069
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
JUGLANS CALIFORNICA POLLEN (JUGLANS CALIFORNICA POLLEN) JUGLANS CALIFORNICA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3069-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3069-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3069-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3069-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
ENGLISH WALNUT english walnut injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3077
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
JUGLANS REGIA POLLEN (JUGLANS REGIA POLLEN) JUGLANS REGIA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3077-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3077-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3077-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3077-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
BLACK WILLOW black willow injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3085
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SALIX NIGRA POLLEN (SALIX NIGRA) SALIX NIGRA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3085-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3085-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3085-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3085-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
ARROYO WILLOW arroyo willow injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3093
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SALIX LASIOLEPIS POLLEN (SALIX LASIOLEPIS POLLEN) SALIX LASIOLEPIS POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3093-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3093-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3093-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3093-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
PUSSY WILLOW pussy willow injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3101
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SALIX DISCOLOR POLLEN (SALIX DISCOLOR POLLEN) SALIX DISCOLOR POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3101-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3101-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3101-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3101-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
POPLAR poplar injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3109
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POPULUS DELTOIDES POLLEN (POPULUS DELTOIDES POLLEN) POPULUS DELTOIDES POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3109-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3109-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3109-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3109-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
BALSAM POPLAR balsam poplar injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:36987-3117
Route of Administration INTRADERMAL, SUBCUTANEOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POPULUS BALSAMIFERA SUBSP. TRICHOCARPA POLLEN (POPULUS BALSAMIFERA SUBSP. TRICHOCARPA POLLEN) POPULUS BALSAMIFERA SUBSP. TRICHOCARPA POLLEN 10000 [PNU] in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE
SODIUM BICARBONATE
WATER
PHENOL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:36987-3117-1 5 mL in 1 VIAL, MULTI-DOSE None
2 NDC:36987-3117-2 10 mL in 1 VIAL, MULTI-DOSE None
3 NDC:36987-3117-3 30 mL in 1 VIAL, MULTI-DOSE None
4 NDC:36987-3117-4 50 mL in 1 VIAL, MULTI-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA102192 08/29/1972
Labeler — Nelco Laboratories, Inc. (054980867)
Registrant — Nelco Laboratories, Inc. (054980867)
Establishment
Name Address ID/FEI Operations
Nelco Laboratories, Inc. 054980867 manufacture

Revised: 12/2009 Nelco Laboratories, Inc.

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