"62795-1011-3" National Drug Code (NDC)

NDC Code	62795-1011-3
Package Description	1 BOTTLE in 1 CARTON (62795-1011-3) / 100 TABLET in 1 BOTTLE
Product NDC	62795-1011
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Bhi Allergy
Non-Proprietary Name	Antimony Trisulfide, Arnica Montana Root, Formic Acid, Graphite, Histamine Dihydrochloride,strychnos Ignatii Seed, Arctium Lappa Root, Ledum Palustre Twig, Lycopodium Clavatum Spore, Pine Tar, Selenium, Sulfur, Sulfuric Acid, Tellurium, Thuja Occidentalis Leafy Twig
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20140830
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	MediNatura
Substance Name	ANTIMONY TRISULFIDE; ARCTIUM LAPPA ROOT; ARNICA MONTANA ROOT; FORMIC ACID; GRAPHITE; HISTAMINE DIHYDROCHLORIDE; LEDUM PALUSTRE TWIG; LYCOPODIUM CLAVATUM SPORE; PINE TAR; SELENIUM; STRYCHNOS IGNATII SEED; SULFUR; SULFURIC ACID; TELLURIUM; THUJA OCCIDENTALIS LEAFY TWIG
Strength	10; 8; 6; 8; 10; 8; 8; 6; 10; 12; 6; 12; 30; 10; 6
Strength Unit	[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1