Miracle Rub
FDA Label NDC 66391-0603

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Winning Solutions for the product Miracle Rub (NDC 66391-0603). 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 otc - active ingredient, otc - purpose, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, indications & usage, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active Ingredient : Menthol  , Methyl Salicylate


Otc - Purpose

Purpose :  External Analgesic

Warnings

Warnings : For external use only

Otc - Keep Out Of Reach Of Children

Keep Out of Reach of Children :  In case of accidental ingestion , get medical help or contact a Position Control center right away.

Dosage & Administration

Directions : adults and children 12 years and older ; apply to affected area no more than 3 to 4 times daily                               under 12 years: ask a doctor before use

Inactive Ingredient

Inactive Ingredients : aloe barbadensis leaf juice , water , stearic acid , cetyl alcohol , glyceryl stearate (and) PEG-100 stearate , petrolatum , dimethicone, triethanolamine , eucalyptus globulus leaf oil ,  imidazolidinyl urea,  methylparaben , propylparaben

Indications & Usage

Uses : Temporarily relieves minor aches and pains of muscles and joints due to  * arthritis  * simple backache  * strains * sprains * bruises

Package Label.Principal Display Panel

 

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