Menthol Overnight Pain Relief Gel-Patch

Menthol Overnight Pain Relief Gel-Patch is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83602-123, application 505G(a)(3), label effective 20260517. 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: temporarily relieves, muscle soreness, minor joint, wrist knees, back neck, hips shoulders. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, back, neck, hips, shoulders, elbows.

Directions Adult and Children above 12 years old: ■ Clean and dry the affected area. ■ Tear off the protective film and apply the exposed part of the patch to the affected area. ■ Carefully remove remaining film while pressing the patch firmly on the skin. ■ Remove patch from the skin after at most 8-hour application. Children under age of 12: Consult a doctor

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 Overnight Pain Relief Gel-Patch used for?
Uses Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, back, neck, hips, shoulders, elbows.

Who makes Menthol Overnight Pain Relief Gel-Patch?
Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. is the labeler of record for Menthol Overnight 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 Overnight 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 Overnight 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 Overnight 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.