Total Muscle Relief
FDA Label NDC 73278-101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Nemadji Management Llc for the product Total Muscle Relief (NDC 73278-101). 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 active ingredients, purpose, warnings, otc - keep out of reach of children, uses, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

MENTHOL  3.9%

cAMPHOR  0.4%

Purpose

TOPICAL ANALGESIC

Warnings

EXTERNAL USE ONLY

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

Uses

TOPICAL RELIEF MUSCLE GEL

Directions

FOR ADULTS AND CHILDREN 2 YEARS AND OLDER. ROLL GEL ONTO AFFECTED AREA, REPEAT AS NEEDED. APPLICATIONS MAY BE REPEATED UP TO 4X DAILY OR AS DIRECTED BY A CARE PROVIDER. FOR CHILDREN UNDER 2 YEARS OF AGE, CONSULT A MEDICAL PROFESSIONAL.

Inactive Ingredients

PURIFIED WATER, ISOPROPYL ALCOHOL, EXTRACT OF ALOE VERA, HEMP GLOWER OIL, WITCH HAZEL AND SAGE, PROPYLENE GLYCOL, GLYCERIN, COCONUT OIL, SWEET ALMOND OIL, DIMETHICONE COPOLYOL SILICA, CARBOMER, TRIETHANOLAMINE, DMDM HYDANTOIN

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