MENTHOL, CAMPHOR

MENTHOL, CAMPHOR is an FDA-registered drug product whose active ingredient is MENTHOL, CAMPHOR. It is labelled by SUNSET PAIN RELIEF taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 72937-013, application M017, label effective 20260820. It is one of 10 FDA drug label records sharing the active ingredient MENTHOL, CAMPHOR. 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, CAMPHOR are most often described in connection with: temporary relief, minor aches, pains muscles, joints associated, simple backache, arthritis sprains. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

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

Directions Adults and Children over 12 years Apply a thin layer to the affected area and rub gently not more than 3 to 4 times a day. Wash hands with soap and water after use. Children under 12 years of age: do not use, consult a doctor.

For external use only. · Ask a doctor before use if you have redness over affected area

FDA lists 10 drug label records with MENTHOL, CAMPHOR 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, CAMPHOR used for?
USE For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, sprains and strains.

Who makes MENTHOL, CAMPHOR?
SUNSET PAIN RELIEF is the labeler of record for MENTHOL, CAMPHOR. 10 FDA label records share the active ingredient MENTHOL, CAMPHOR, 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, CAMPHOR 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, CAMPHOR 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, CAMPHOR?
Yes. 10 FDA drug label records list MENTHOL, CAMPHOR 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, CAMPHOR 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.