FDA.reportPublic FDA data

T Relief Arthritis Tablet

Manufacturer
MediNatura Inc
Effective date
2023-08-07
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 02:21:59

Label at a glance#

ProductT Relief Arthritis
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

Relieves 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#

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

WARNINGS

WARNINGS SECTION

Warnings: If pregnant or breatfeeding, ask health proffessional. 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-Relief™ Arthritis or any of its ingredients exists.

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Each tablet contains: *Dulcamara
2X 5mg, *Arnica montana 3X 10mg, *Sanguinaria
canadensis 3X 0.5mg,*Bryonia alba 3X 0.3mg, *Cartilago
suis 4X 0.3mg,*Rhus toxicodendron 4X 5mg, *Sulphur
6X 5mg,*Ledum palustre 6X 4mg,*Bryonia alba 6X
0.3mg, *Embryo suis 6X 0.3mg,*Funiculus umbilicalis
suis 6X 0.3mg, *Placenta totalis suis 6X 0.3mg,
*Symphytum officinale 7X 0.02mg, *Rhododendron
chrysanthum 8X 0.3mg, *Bryonia alba 12X 0.3mg.
*Natural Ingredient

Uses

INDICATIONS & USAGE SECTION

Relieves

  • Arthritis pain
  • Joint pain
  • Joint stiffness

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Dextrose, Maltodextrin Magnesium stearate. 

PURPOSE

OTC - PURPOSE SECTION

Uses: For the temporary relief of minor: Arthritis pain, Joint pain, Joint stiffness

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 TabletT Relief Arthritis Tablet

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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
62795-1033-22026-01-29C16284748780-149896155-a0da-586f-e063-e6dba90add90T Relief Arthritis Tablet
62795-1033-42026-01-29C16284748780-149896155-a0da-586f-e063-e6dba90add90T Relief Arthritis Tablet

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62795-1033-2T Relief Arthritis100 in 1 BOTTLETABLET1009
62795-1033-2T Relief Arthritis1 in 1 CARTONTABLET19
62795-1033-4T Relief Arthritis100 in 1 BOTTLETABLET1009

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62795-1033T RELIEF ARTHRITIS (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]9Legacy NDC, 3 package rows20230808_56921554-9252-4f47-afe0-75d38bd4498c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62795-1033-2EA - Each62795-1033c3baca51-d826-42a1-b8f8-dca1fcdcf78812018-10-11

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62795-103362795-1033-2, 62795-1033-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
MAGNESIUM STEARATE70097M6I30IACT
ARNICA MONTANAO80TY208ZWACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
SUS SCROFA CARTILAGE73ECW5WG2FACTIB
SOLANUM DULCAMARA TOPKPS1B1162NACTIB
SUS SCROFA EMBRYO9928MC12VOACTIB
SUS SCROFA UMBILICAL CORD118OYG6W3HACTIB
LEDUM PALUSTRE TWIG877L01IZ0PACTIB
SUS SCROFA PLACENTAC8CV8867O8ACTIB
RHODODENDRON AUREUM LEAFIV92NQJ73UACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
SANGUINARIA CANADENSIS ROOTN9288CD508ACTIB
SULFUR70FD1KFU70ACTIB
COMFREY ROOTM9VVZ08EKQACTIB
DEXTROSEIY9XDZ35W2IACT
MALTODEXTRIN7CVR7L4A2DIACT

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
79c60c29-1a43-420c-bcf4-1adea6445e2256921554-9252-4f47-afe0-75d38bd4498c2023-08-07WarningsExact identifier
spl id: 79c60c29-1a43-420c-bcf4-1adea6445e22
spl set id: 56921554-9252-4f47-afe0-75d38bd4498c

Reported adverse events (FAERS/openFDA)#

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