MG PLUS ROLL ON

MG PLUS ROLL ON is an FDA-registered drug product whose active ingredient is MENTHOL ROLL ON. It is labelled by RENU LABORATORIES, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 76348-971, application M017, label effective 20260603. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing MENTHOL ROLL ON are most often described in connection with: bandage tightly, avoid contact, apply wounds, damaged skin, heating pads. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

When using this product Do not bandage tightly avoid contact with eyes do not apply to wounds or damaged skin do not use with heating pads or other heating devices

Uses for the temporary relief of minor aches and pains associated with sore muscles, joint discomfort, strains, sprains, bruises and arthritis Directions adults and children 12 years of age and older, apply to affected areas no more than 10 times a day as needed for pain children under 12 years of age: do not use, consult a doctor.

Warnings For external use only

What is MG PLUS ROLL ON used for?
When using this product Do not bandage tightly avoid contact with eyes do not apply to wounds or damaged skin do not use with heating pads or other heating devices

Who makes MG PLUS ROLL ON?
RENU LABORATORIES, LLC is the labeler of record for MG PLUS ROLL ON.

What form does MG PLUS ROLL ON come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is MG PLUS ROLL ON prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has MG PLUS ROLL ON been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.