T-Relief Extra Strength Gel

Manufacturer
MediNatura Inc
Effective date
2023-09-27
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:22:26

Label at a glance#

ProductT-Relief Extra Strength Gel
Active ingredientACONITUM NAPELLUS, ARNICA MONTANA, BAPTISIA TINCTORIA ROOT, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, ECHINACEA, UNSPECIFIED, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, HYPERICUM PERFORATUM, ACHILLEA MILLEFOLIUM, RUTA GRAVEOLENS FLOWERING TOP, COMFREY ROOT
Label structure8 sections

Indications and uses

For the temporary relief of minor: Joint Pain • Back Pain • Muscular Pain • Nerve Pain, Arthritis Pain

Dosage and administration

Twist off cap and remove the foil seal. Adults and children 4 years and older: Apply generously to affected areas 2 to 3 times daily, or more often if necessary. Massage thoroughly into the skin. If appropriate, mild compression or occlusive bandaging may be applied. For children under 4,consult your health professional.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Purpose

*Aconitum napellus 1X 0.08%................Reduces joint and back pain

*Arnica montana 1X 3.3%........Reduces Arthritis and back pain

*Arnica montana 3X 2.51%..........Reduces Arthritis and back pain

*Arnica montana10X 0.12%........Reduces Arthritis and back pain

*Wild Harvest Baptisia tinctoria 4X 0.75% ..................Relieves joint and muscle soreness

*Belladonna 2X 0.75%...........................Reduces back pain

*Bellis perennis 2X 0.75%......................Relieves joint and muscle soreness

*Organic Calendula officinalis 1X 2.51%..............Relieves pain

*Organic Chamomilla 2X 0.91%.........................Soothing pain relief

*Organic Echinacea 1X 0.75%............................Relieves pain

*Hamamelis virginiana 2X 2.26%...........Relieves joint and muscle soreness

*Hypericum perforatum 6X 0.12%.........Reduces nerve pain

*Organic Millefolium 2X 2.71%...........................Relieves pain

*Ruta graveolens 4X 3%..................Relieves pain

*Symphytum officinale 4X 0.15%..........Relieves joint pain

*Natural. T-Relief Extra Strength contains 50 % more each medicine than regular T-Relief.

USES

OTC - PURPOSE SECTION

For the temporary relief of minor: Joint Pain • Back Pain • Muscular Pain • Nerve Pain, Arthritis Pain

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS

INDICATIONS & USAGE SECTION

For the temporary relief of minor: Joint Pain • Back Pain • Muscular Pain • Nerve Pain, Arthritis Pain

WARNINGS

WARNINGS SECTION

For external use only. Do not apply over open wounds or broken skin. If symptoms persist or worsen, or if a rash develops, a health professional should be consulted. In rare cases, allergic skin reactions may develop. Do not use if known sensitivity to T-ReliefTM or any of its ingredients exists.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Twist off cap and remove the foil seal.

Adults and children 4 years and older: Apply generously to affected areas 2 to 3 times daily, or more often if necessary. Massage thoroughly into the skin. If appropriate, mild compression or occlusive bandaging may be applied.

For children under 4,consult your health professional.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Carbomer 980, Organic ethanol, Phenoxyethanol, Purified Water, SD Alcohol , Sodium Hydroxide.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

T-Relief Extra Strength Gel.jpgT-Relief Extra Strength Gel.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62795-7006-4T-Relief Extra Strength Gel1 in 1 CARTONGEL15
62795-7006-4T-Relief Extra Strength Gel85 g in 1 TUBEGEL855

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62795-7006T-RELIEF EXTRA STRENGTH GEL (ACONITUM NAPELLUS, ARNICA MONTANA, BAPTISIA TINCTORIA ROOT, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, ECHINACEA UNSPECIFIED, HAMAMELIS VIRGINIANA ROOT BARK STEM BARK, HYPERICUM PERFORATUM, ACHILLEA MILLEFOLIUM, RUTA GRAVEOLENS FLOWERING TOP AND COMFREY ROOT) GEL [MEDINATURA INC]5Current NDC, Legacy NDC, 2 package rows20231004_e4bf2e39-5635-4797-8519-7e115e8b1a27.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62795-7006-4GM - Gram62795-700634dacdfc-8014-488e-9660-0f0852fea99212022-05-04

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62795-700662795-7006-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
T-Relief Extra Strength GelACONITUM NAPELLUS, ARNICA MONTANA, BAPTISIA TINCTORIA ROOT, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, ECHINACEA UNSPECIFIED, HAMAMELIS VIRGINIANA ROOT BARK STEM BARK, HYPERICUM PERFORATUM, ACHILLEA MILLEFOLIUM, RUTA GRAVEOLENS FLOWERING TOP AND COMFREY ROOTMediNatura Ince4bf2e39-5635-4797-8519-7e115e8b1a272023-09-27WarningsExact identifier
ndc (package): 62795-7006-4
ndc (product): 62795-7006
ndc11 (package): 62795700604
spl id: 0747964b-b515-47b6-87ac-542b263a54a4
spl set id: e4bf2e39-5635-4797-8519-7e115e8b1a27

Reported adverse events (FAERS/openFDA)#

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