BeeVenom

BeeVenom is an FDA-registered drug product whose active ingredient is METHYL SALICYLATE. It is labelled by Menper Distributors, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 53145-315, application M017, label effective 20260420. It is one of 5 FDA drug label records sharing the active ingredient METHYL SALICYLATE. 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 METHYL SALICYLATE 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 and sprains.

Directions: use only as directed Adults and children 2 years and older: apply to affected area not more than 3 to 4 time daily children under 12 years of age: ask a doctor

Warnings For external use only

FDA lists 5 drug label records with METHYL SALICYLATE 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 BeeVenom used for?
Uses For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains and sprains.

Who makes BeeVenom?
Menper Distributors, Inc. is the labeler of record for BeeVenom. 5 FDA label records share the active ingredient METHYL SALICYLATE, 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 BeeVenom 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 BeeVenom 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 METHYL SALICYLATE?
Yes. 5 FDA drug label records list METHYL SALICYLATE 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 BeeVenom 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.