"50114-6165-2" National Drug Code (NDC)

NDC Code	50114-6165-2
Package Description	100 TABLET in 1 BOTTLE (50114-6165-2)
Product NDC	50114-6165
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Zeel
Non-Proprietary Name	.alpha.-lipoic Acid, Arnica Montana Root, Sus Scrofa Cartilage, Coenzyme A, Solanum Dulcamara Top, Sus Scrofa Embryo, Sus Scrofa Umbilical Cord, Nadide, Sodium Diethyl Oxalacetate, Sus Scrofa Placenta, Toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Silicon Dioxide, Sulfur And Comfrey Root
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19840131
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Heel Inc.
Substance Name	.ALPHA.-LIPOIC ACID; ARNICA MONTANA ROOT; COENZYME A; COMFREY ROOT; NADIDE; SANGUINARIA CANADENSIS ROOT; SILICON DIOXIDE; SODIUM DIETHYL OXALACETATE; SOLANUM DULCAMARA TOP; SULFUR; SUS SCROFA CARTILAGE; SUS SCROFA EMBRYO; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; TOXICODENDRON PUBESCENS LEAF
Strength	6; 1; 6; 8; 6; 3; 6; 6; 2; 6; 4; 4; 4; 4; 1
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