"43857-0011-1" National Drug Code (NDC)

NDC Code	43857-0011-1
Package Description	30 mL in 1 BOTTLE, DROPPER (43857-0011-1)
Product NDC	43857-0011
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Candida Combo
Non-Proprietary Name	Candida Albicans
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20130116
End Marketing Date	20250127
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	BioActive Nutritional, Inc.
Substance Name	CANDIDA ALBICANS
Strength	12
Strength Unit	[hp_X]/mL
Pharmacy Classes	Allergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC]