"63083-4017-2" National Drug Code (NDC)

NDC Code	63083-4017-2
Package Description	59 mL in 1 BOTTLE, DROPPER (63083-4017-2)
Product NDC	63083-4017
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Allergy Nosode
Proprietary Name Suffix	4017
Non-Proprietary Name	Allergy Nosode
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	19840815
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Professional Complementary Health Formulas
Substance Name	CALCIUM SULFIDE; FRAXINUS LATIFOLIA WHOLE; GUAIAC; HISTAMINE; HOUSE DUST; LUFFA OPERCULATA FRUIT; MEDICAGO SATIVA WHOLE; POTASSIUM DICHROMATE; SILICON DIOXIDE; STACHYBOTRYS CHARTARUM; TARAXACUM OFFICINALE
Strength	12; 12; 6; 12; 12; 6; 12; 30; 12; 12; 12
Strength Unit	[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacy Classes	Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Fungal Proteins [CS], House Dust [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized House Dust Allergenic Extract [EPC]