OVERNIGHT RELIEF Gel-Patch

OVERNIGHT 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 73557-134, 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: temporarily relieves, minor aches, pains muscles, joints associated, simple backache, arthrits strains, bruises sprains. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Temporarily relieves minor aches and pains of muscles and joints associated with: simple backache arthrits strains bruises sprains

Directions • adults and children 12 years of age and older: Clean and dry affected area, pop apart and partially peel back protective film and apply exposed gel-patch to site of pain. Carefully remove remaining film while pressing the gel-patch to skin and leave in place for up to 8 hours. Use on affected areas not more than 3 to 4 times daily. • children under 12 years of age: consult a physician • wash hands after use with cool water

Warnings For external use only When using this prudocts : • use only as directed • avoid contact with eyes or on mucous membranes • do not apply to wounds or damaged skin • do not apply to irritated skin or if excessive irritation develops • do not bandage tightly or use with heating pad or device Stop use and ask a doctor if: • you experience pain, swelling or blistering of the skin • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days • arthritic pain persists for more than 10 days, or redness is present If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. If accidentally ingested, get medical help or contact a Poison Control Center immediately

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 OVERNIGHT RELIEF Gel-Patch used for?
Uses Temporarily relieves minor aches and pains of muscles and joints associated with: simple backache arthrits strains bruises sprains

Who makes OVERNIGHT RELIEF Gel-Patch?
Shanghai Chuangshi Medical Technology (Group) Co., Ltd. is the labeler of record for OVERNIGHT 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 OVERNIGHT 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 OVERNIGHT 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 OVERNIGHT 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.