"50114-7030-1" National Drug Code (NDC)

NDC Code	50114-7030-1
Package Description	10 AMPULE in 1 CARTON (50114-7030-1) > 2 mL in 1 AMPULE
Product NDC	50114-7030
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Zeel
Non-Proprietary Name	Arnica Montana Root, Toxicodendron Pubescens Leaf, Solanum Dulcamara Top, Comfrey Root, Sulfur, Sanguinaria Canadensis Root, Sus Scrofa Cartilage, Sus Scrofa Embryo, Sus Scrofa Umbilical Cord, Sus Scrofa Placenta, .alpha.-lipoic Acid, Coenzyme A, Nadide And Sodium Diethyl Oxalacetate
Dosage Form	INJECTION
Usage	INTRA-ARTICULAR; INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date	20140731
End Marketing Date	20241231
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	MediNatura
Substance Name	.ALPHA.-LIPOIC ACID; ARNICA MONTANA ROOT; COENZYME A; COMFREY ROOT; NADIDE; SANGUINARIA CANADENSIS ROOT; SODIUM DIETHYL OXALACETATE; SOLANUM DULCAMARA TOP; SULFUR; SUS SCROFA CARTILAGE; SUS SCROFA EMBRYO; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; TOXICODENDRON PUBESCENS LEAF
Strength	8; 4; 8; 6; 8; 4; 8; 3; 6; 6; 6; 6; 6; 2
Strength Unit	[hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL