T-relief Extra Strength Tablet, Chewable
FDA Label NDC 62795-1041

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 62795-1041). 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, indications, ingredients, inactive ingredient, 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 or any of its ingredients exists

Uses

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

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Indications

Relieves muscle, Joint, back, nerve and arthritis pain.

Ingredients

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

Inactive Ingredient

Lactose, Magnesium stearate

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