"50114-4286-2" National Drug Code (NDC)

NDC Code	50114-4286-2
Package Description	100 TABLET in 1 BOTTLE (50114-4286-2)
Product NDC	50114-4286
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	19930131
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Heel Inc
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; 19; 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