"50181-0014-1" National Drug Code (NDC)

NDC Code	50181-0014-1
Package Description	30 mL in 1 BOTTLE, DROPPER (50181-0014-1)
Product NDC	50181-0014
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Biotox Para
Non-Proprietary Name	Cochlearia Armoracia, Toxoplasma Gondii, Vibrio Cholerae, Candida Albicans, Trichinella Spiralis
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20130607
End Marketing Date	20251007
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	The Wellness Center
Substance Name	CANDIDA ALBICANS; HORSERADISH; PLASMODIUM MALARIAE; TARAXACUM OFFICINALE; TOXOPLASMA GONDII; TRICHINELLA SPIRALIS; TRICHOPHYTON RUBRUM; VIBRIO CHOLERAE
Strength	30; 3; 12; 8; 12; 30; 200; 30
Strength Unit	[hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL
Pharmacy Classes	Allergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Fungal Proteins [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]