T-relief Extra Strength Solution/ Drops
FDA Label NDC 62795-2010

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Medinatura Inc for the product T-relief Extra Strength (NDC 62795-2010). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding warnings, uses, keep out of reach of children, purpose, directions, inactive ingredients, active ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Warnings

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.

Uses

Uses

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

Keep Out Of Reach Of Children

If symptoms persist or worsen, a health professional should be consulted .

Purpose

Relieves

• Joint Pain

• Back Pain

• Muscular Pain

Directions

Adults and children 12 years and older: 10 drops every 4 hours not exceed 60 drops per 24 hours. For children under 12 years: Consult your health professional.

Inactive Ingredients

Ethanol, Purified water

Active Ingredients

Each 50mL contains: *Arnica montana 3X 42%,
Wild-Harvested Baptisia tinctoria 2X 9%, *Aconitum napellus 3X 7.5%,
*Symphytum officinale 8X 7.5%, Organic Millefolium 2X 6%, *Ruta
graveolens 3X 4%, *Arnica montana 4X 3.6%, *Arnica montana 8X 3.6%,
*Bellis perennis 2X 3%, Organic Calendula officinalis 2X 3%, Organic
Echinacea 2X 3%, *Hamamelis virginiana 2X 3%, *Hypericum perforatum
3X 3%, *Belladonna 3X 0.9%, Organic Chamomilla 2X 0.9%

* Please review the disclaimer below.