MENTHOL PAIN RELIEF Gel-Patch

MENTHOL PAIN RELIEF Gel-Patch is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by Shanghai Chuangshi Medical Technology (Group) Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 73557-131, application 505G(a)(3), label effective 20260514. It is one of 193 FDA drug label records sharing the active ingredient MENTHOL. 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 are most often described in connection with: temporary relief, minor aches, pains sore, joints associated, arthrits backache, strains sprains. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses: Temporary relief from minor aches and pains of sore muscles and joints associated with: · arthrits · backache · strains · sprains

Directions · Adult and Children 12 years of age and older: Clean and dry affected area, partially peel back protective film and apply exposed patch to site of pain. Carefully remove remaining film while pressing patch to skin and leave in place for up to 8 hours. Use on affected areas not more than 4 times daily. Wash hands with cool water after use. · Children under 12 years of age : Consult physician

Warnings For external use only

FDA lists 193 drug label records with MENTHOL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is MENTHOL PAIN RELIEF Gel-Patch used for?
Uses: Temporary relief from minor aches and pains of sore muscles and joints associated with: · arthrits · backache · strains · sprains

Who makes MENTHOL PAIN RELIEF Gel-Patch?
Shanghai Chuangshi Medical Technology (Group) Co., Ltd. is the labeler of record for MENTHOL PAIN RELIEF Gel-Patch. 193 FDA label records share the active ingredient MENTHOL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does MENTHOL PAIN RELIEF Gel-Patch 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 MENTHOL PAIN RELIEF Gel-Patch 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.

Are there other products containing MENTHOL?
Yes. 193 FDA drug label records list MENTHOL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has MENTHOL PAIN RELIEF Gel-Patch 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.