"62795-1039-2" National Drug Code (NDC)

NDC Code	62795-1039-2
Package Description	100 TABLET in 1 PACKAGE (62795-1039-2)
Product NDC	62795-1039
Product Type Name	HUMAN OTC DRUG
Proprietary Name	T-relief Pro Arthritis
Non-Proprietary Name	Arnica Montana, Bryonia Alba Whole, Sus Scrofa Cartilage,solanum Dulcamara Top,sus Scrofa Embryo,sus Scrofa Umbilical Cord,rhododendron Tomentosum Leafy Twig,sus Scrofa Placenta,rhododendron Aureum Leaf,toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Sulfur And Comfrey Root
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20171213
End Marketing Date	20260327
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	MediNatura Inc
Substance Name	ARNICA MONTANA; BRYONIA ALBA WHOLE; COMFREY ROOT; RHODODENDRON AUREUM LEAF; RHODODENDRON TOMENTOSUM LEAFY TWIG; SANGUINARIA CANADENSIS ROOT; SOLANUM DULCAMARA TOP; SULFUR; SUS SCROFA CARTILAGE; SUS SCROFA EMBRYO; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; TOXICODENDRON PUBESCENS LEAF
Strength	3; 3; 7; 8; 6; 3; 2; 6; 4; 6; 6; 6; 4
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