"62795-9494-2" National Drug Code (NDC)

NDC Code	62795-9494-2
Package Description	1 BOTTLE in 1 CARTON (62795-9494-2) / 100 TABLET in 1 BOTTLE
Product NDC	62795-9494
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Zeel
Non-Proprietary Name	Alpha Lipoic Acid, Arnica Montanaroot,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,comfrey Root
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20220112
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	MediNatura 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; 2
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