T Relief Arthritis Extra Strength

Manufacturer
MediNatura Inc
Effective date
2023-09-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:22:22

Label at a glance#

ProductT Relief Arthritis Extra Strength
Active ingredientARNICA MONTANA, BRYONIA ALBA ROOT, SUS SCROFA CARTILAGE, SOLANUM DULCAMARA TOP, SUS SCROFA EMBRYO, SUS SCROFA UMBILICAL CORD, LEDUM PALUSTRE TWIG, SUS SCROFA PLACENTA, RHODODENDRON AUREUM LEAF, TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SULFUR, COMFREY ROOT
Label structure8 sections

Indications and uses

 For the temporary relief of minor: Arthritis Pain • Joint Pain • Joint Stiffness

Dosage and administration

For max absorption, dissolve under tongue. Can be chewed and swallowed. Adults: 2 tablets every 4 hours. Do not exceed 12 tablets per 24 hours. Children under 18 years: consult your health professional

Label contents#

Full prescribing information#

Warnings:

WARNINGS SECTION

 If pregnant or breast-feeding, ask a health
professional. Keep out of reach of children.
If symptoms persist or worsen, a health professional
should be consulted. Do not use if known sensitivity to
T-ReliefTM Arthritis or any of its ingredients exists.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

 *Dulcamara 2X 7.5mg, *Arnica
montana 3X 15mg, *Sanguinaria canadensis 3X 0.75mg,
*Bryonia alba 3X, 6X, 12X 0.45mg each, *Rhus
toxicodendron 4X 7.5mg, *Cartilago suis 4X 0.45mg,
*Sulphur 6X 7.5mg,*Ledum palustre 6X 6mg,*Embryo suis
6X 0.45mg,*Funiculus umbilicalis suis 6X 0.45mg,
*Placenta totalis suis 6X 0.45mg, *Symphytum officinale 7X
0.03mg, *Rhododendron chrysanthum 8X 0.45mg.
T-ReliefTM Arthritis Extra Strength contains 50% more of
each pain reliever than regular T-ReliefTM Arthritis. *Natural

Uses:

INDICATIONS & USAGE SECTION

 For the temporary relief of minor:
Arthritis Pain • Joint Pain • Joint Stiffness

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

 *Dextrose, *Lactose,
Magnesium stearate, *Maltodextrin
*contains one or more of these ingredients

Purpose

OTC - PURPOSE SECTION

PAIN RELIEF

Directions:

DOSAGE & ADMINISTRATION SECTION

For max absorption, dissolve under tongue.
Can be chewed and swallowed. Adults: 2 tablets every
4 hours. Do not exceed 12 tablets per 24 hours.
Children under 18 years: consult your health professional

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

T Relief Arthritis Extra Strength.jpgT Relief Arthritis Extra Strength.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62795-1053-22025-01-30C16284748780-12cef2736-9b53-d83d-e063-dadaa90ab31fT Relief Arthritis Extra Strength

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62795-1053-2T Relief Arthritis Extra Strength250 in 1 BOTTLETABLET2502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62795-1053T RELIEF ARTHRITIS EXTRA STRENGTH (ARNICA MONTANA, BRYONIA ALBA ROOT, SUS SCROFA CARTILAGE, SOLANUM DULCAMARA TOP, SUS SCROFA EMBRYO,SUS SCROFA UMBILICAL CORD, LEDUM PALUSTRE TWIG,SUS SCROFA UMBILICAL CORD, LEDUM PALUSTRE TWIG,SUS SCROFA PLACENTA, RHODODENDRON AUREUM LEAF,TOXICODENDRON PUBESCENS LEAF, SANGUINARIA CANADENSIS ROOT, SULFUR, AND COMFREY ROOT) TABLET [MEDINATURA INC]2Legacy NDC, 1 package rows20230928_dbfd6183-a058-4292-ab99-31a60b1dd215.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62795-1053-2EA - Each62795-1053b2f0dd63-685e-4b1f-a22d-7123c031db8712022-05-04

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62795-105362795-1053-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5b85f305-4463-4a4e-ac6f-c3265fcc96ccdbfd6183-a058-4292-ab99-31a60b1dd2152023-09-27WarningsExact identifier
spl id: 5b85f305-4463-4a4e-ac6f-c3265fcc96cc
spl set id: dbfd6183-a058-4292-ab99-31a60b1dd215

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.