FDA.reportPublic FDA data

T-Relief Pro

Manufacturer
MediNatura Inc
Effective date
2021-06-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:41:36

Label at a glance#

ProductT-Relief Pro
Active ingredientARNICA MONTANA, ACONITUM NAPELLUS, BAPTISIA TINCTORIA ROOT, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA CHAMOMILLA, 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: • Pain relief tablets , inflammation • Joint Pain, Muscular Pain • Bruising • Sports injuries • Sprains

Dosage and administration

Adults and children 12 years and older: Chew 2 tablet every 4 hours or as directed by health professional. Children 4 to 11 years: Chew 1 to 2 tablets every 4 hours or as directed by health professional. For children under 4 years: use as directed by your health professional.

Label contents#

Full prescribing information#

USES

INDICATIONS & USAGE SECTION

For the temporary relief of minor:
• Pain relief tablets , inflammation
• Joint Pain, Muscular Pain
• Bruising
• Sports injuries
• Sprains

WARNINGS

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use. 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 or any of its ingredients exists

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and older: Chew 2 tablet every 4 hours or as directed by health professional. Children 4 to 11 years: Chew 1 to 2 tablets every 4 hours or as directed by health professional. For children under 4 years: use as directed by your health professional.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Lactose, Magnesium stearate

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS

OTC - PURPOSE SECTION

For the treatment of minor: inflammation, Joint , back& Muscular Pain. Bruising* Sports injuries* Sprains.

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Aconitum napellus 3X 12.5%, Arnica montana 3X 62%, Arnica montana 4X 0.09%, Arnica montana 8X 0.03%, Baptisia tinctoria 2X 2.5%, Belladonna 3X 3.3%, Bellis perennis 2X 2.50%, Calendula officinalis 2X 4%, Chamomilla 2X 1.3%, Echinacea 2X 2.50%, Hamamelis virginiana 2X 4%, Hypericum perforatum 3X 3%, Millefolium 2X 0.8%, Ruta graveolens 3X 0.4%, Symphytum officinale 6X 0.1%.

T-Relief Pro

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

T-Relief Pro.jpgT-Relief Pro.jpg

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62795-1038T-RELIEF PRO (ACONITUM NAPELLUS, ARNICA MONTANA, BAPTISIA TINCTORIA ROOT, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA CHAMOMILLA, ECHINACEA UNSPECIFIED, HAMAMELIS VIRGINIANA ROOT BARK STEM, HYPERICUM PERFORATUM, RUTA GRAVEOLENS FLOWERING TOP, ACHILLEA MILLEFOLIUM AND COMFREY ROOT) TABLET, CHEWABLE [MEDINATURA INC]3Legacy NDC20210701_1f10a536-a711-4c5b-8ff0-77577653ca36.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62795-1038-2EA - Each62795-1038bf6b4cdf-de94-4fc3-858e-2288414ba07212018-12-13

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62795-103862795-1038-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARNICA MONTANAO80TY208ZWACTIB
ACONITUM NAPELLUSU0NQ8555JDACTIB
BAPTISIA TINCTORIA ROOT5EF0HWI5WUACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
BELLIS PERENNIS2HU33I03UYACTIB
CALENDULA OFFICINALIS FLOWERING TOP18E7415PXQACTIB
MATRICARIA CHAMOMILLAG0R4UBI2ZZACTIB
ECHINACEA, UNSPECIFIED4N9P6CC1DXACTIB
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARKT7S323PKJSACTIB
HYPERICUM PERFORATUMXK4IUX8MNBACTIB
ACHILLEA MILLEFOLIUM2FXJ6SW4PKACTIB
RUTA GRAVEOLENS FLOWERING TOPN94C2U587SACTIB
COMFREY ROOTM9VVZ08EKQACTIB
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
MAGNESIUM STEARATE70097M6I30IACT

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
4af5462c-6cf2-4fd1-af4e-429b398c917c1f10a536-a711-4c5b-8ff0-77577653ca362021-06-29WarningsExact identifier
spl id: 4af5462c-6cf2-4fd1-af4e-429b398c917c
spl set id: 1f10a536-a711-4c5b-8ff0-77577653ca36

Reported adverse events (FAERS/openFDA)#

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