NDC 62795-1039

T-Relief PRO Arthritis

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

T-Relief PRO Arthritis is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Medinatura Inc. The primary component is 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; Comfrey Root.

Product ID62795-1039_4899dee5-3011-4794-966f-3be10db2dedd
NDC62795-1039
Product TypeHuman Otc Drug
Proprietary NameT-Relief PRO Arthritis
Generic NameArnica 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 FormTablet
Route of AdministrationORAL
Marketing Start Date2017-12-13
Marketing End Date2026-03-27
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameMediNatura Inc
Substance NameARNICA 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; COMFREY ROOT
Active Ingredient Strength3 [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
NDC Exclude FlagN

Packaging

NDC 62795-1039-2

100 TABLET in 1 PACKAGE (62795-1039-2)
Marketing Start Date2017-12-13
Marketing End Date2026-03-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62795-1039-2 [62795103902]

T-Relief PRO Arthritis TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2017-12-13

Drug Details

Active Ingredients

IngredientStrength
ARNICA MONTANA3 [hp_X]/1

OpenFDA Data

SPL SET ID:312cabae-6b7e-401b-9284-f71f8a921e91
Manufacturer
UNII
UPC Code
  • 0787647852567

  • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.