"51885-9489-8" National Drug Code (NDC)

NDC Code	51885-9489-8
Package Description	1 TUBE in 1 CARTON (51885-9489-8) / 100 g in 1 TUBE
Product NDC	51885-9489
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Zeel
Non-Proprietary Name	Alpha Lipoic Acid, Arnica Montana Whole,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,coriander
Dosage Form	OINTMENT
Usage	TOPICAL
Start Marketing Date	20210922
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Biologische Heilmittel Heel
Substance Name	ALPHA LIPOIC ACID; ARNICA MONTANA WHOLE; COENZYME A; CORIANDER; 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; 2; 6; 8; 6; 2; 6; 6; 2; 6; 2; 2; 2; 2; 2
Strength Unit	[hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g