T-Relief Oral Drop

Manufacturer
MediNatura Inc
Effective date
2018-10-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 00:48:49

Label at a glance#

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

Indications and uses

Uses For the temporary relief of minor: Joint Pain, Back Pain, and Muscular Pain

Dosage and administration

At first sign of symptoms: Adults and children 12 years and older: 10 drops every ½ to 1 hour until symptoms lessen, then continue with standard dosage. Do not exceed 120 drops in 24 hours. For children under 12 years: Consult your health professional. Standard Dosage: Adults and children 12 years and older: 30 drops per day, taking 10 drops every 4 to 6 hours . For children under 12 years: Consult your health pro...

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

*Aconitum napellus 3x, *Arnica montana 3X, 6X, 10X, Baptisia tinctoria 2X, Belladonna 3X, Bellis perennis 2X, Calendula officinalis 2X, Chamomilla 2X, Echinacea 2X, Hamamelis virginiana 2X, Hypericum perforatum 3X, Millefolium 2X, Ruta graveolens 4X, and Symphytum officinalis 8X

*Natural Ingredients

USES

INDICATIONS & USAGE SECTION

Uses

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

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Ethanol, Purified water

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

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 TM or any of its ingredients exists.

PURPOSE

OTC - PURPOSE SECTION

Relieves

• Joint Pain

• Back Pain

• Muscular Pain

Directions

DOSAGE & ADMINISTRATION SECTION

At first sign of symptoms: Adults and children 12 years and older: 10 drops every ½ to 1 hour until symptoms lessen, then continue with standard dosage. Do not exceed 120 drops in 24 hours. For children under 12 years: Consult your health professional.

Standard Dosage: Adults and children 12 years and older: 30 drops per day, taking 10 drops every 4 to 6 hours . For children under 12 years: Consult your health professional.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

T-Relief Oral Drop.jpgT-Relief Oral Drop.jpg

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codeopn.to/a/ml3NqT-Relief Oral Drop.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62795-2006-42020-02-10C16284748780-19d75b9d0-901c-f424-e053-dadaa90a57ceT-Relief Oral Drop
62795-2006-42020-01-31C16284748780-19d75b9d0-901c-f424-e053-dadaa90a57ceT-Relief Oral Drop

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62795-2006-4ML - Milliliter62795-2006e708e101-2c42-4a3f-865e-0eff626f447f12018-10-11

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
62795-200662795-2006-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
89ff27b5-99a0-4ebf-8ece-efdf9d2196771e15ca0d-d19a-1bd0-e054-00144ff8d46c2018-10-17WarningsExact identifier
spl id: 89ff27b5-99a0-4ebf-8ece-efdf9d219677
spl set id: 1e15ca0d-d19a-1bd0-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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