Meriwether Skin Pain Relief

Meriwether Skin Pain Relief is an FDA-registered drug product whose active ingredient is MENTHOL, UNSPECIFIED FORM. It is labelled by Meriwether Skin LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87860-002, application M017, label effective 20260716. It is one of 17 FDA drug label records sharing the active ingredient MENTHOL, UNSPECIFIED FORM. 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, UNSPECIFIED FORM are most often described in connection with: temporary relief, minor aches, pains muscles, joints associated, simple backache, arthritis strains. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains

Directions Adults and children 2 years of age and older: Apply to affected area not more that 3 to 4 times daily. Children under 2 years of age: do not use, consult a Doctor

Warnings For external use only Do not use To wounds or damaged skin. Do not bandage tightly When using this product Avoid contact with the eyes Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use

FDA lists 17 drug label records with MENTHOL, UNSPECIFIED FORM 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 Meriwether Skin Pain Relief used for?
Uses For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains

Who makes Meriwether Skin Pain Relief?
Meriwether Skin LLC is the labeler of record for Meriwether Skin Pain Relief. 17 FDA label records share the active ingredient MENTHOL, UNSPECIFIED FORM, 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 Meriwether Skin Pain Relief 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 Meriwether Skin Pain Relief 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, UNSPECIFIED FORM?
Yes. 17 FDA drug label records list MENTHOL, UNSPECIFIED FORM 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 Meriwether Skin Pain Relief 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.