T-Relief PRO Arthritis

Product NDC

62795-1039

11-digit product format

627951039

Labeler code

62795

Product ID

62795-1039_4899dee5-3011-4794-966f-3be10db2dedd

Type

HUMAN OTC DRUG

Nonproprietary 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

Route

ORAL

Labeler

MediNatura Inc

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2017-12-13

Marketing end

2026-03-27

Substance

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

Active strength

3 [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 flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record