Crysalo

Crysalo is an FDA-registered drug product whose active ingredient is METHYL SALICYLATE, MENTHOL. It is labelled by V2 Pharma, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 72835-511, label effective 20260706. It is one of 9 FDA drug label records sharing the active ingredient METHYL SALICYLATE, 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 METHYL SALICYLATE, MENTHOL are most often described in connection with: temporary relief, minor aches, pains associated, simple backache, arthritis strains. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Temporary relief of minor aches and pains associated with: Simple backache Arthritis Strains, sprains, and bruises

Directions Adults and children 12 years of age and older: Apply to affected area not more then 3 to 4 times daily. No need to rub in. For children under 12 years of age: Ask a doctor.

Fore external use only. Avoid contact with the eyes. Keep out of reach of children. When using this product Do not apply to wounds or damaged skin. Do not bandage tightly. Do not use with heating pad. Rinse with soap and water to remove. Wash hands with soap and water after use.

FDA lists 9 drug label records with METHYL SALICYLATE, 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 Crysalo used for?
Uses Temporary relief of minor aches and pains associated with: Simple backache Arthritis Strains, sprains, and bruises

Who makes Crysalo?
V2 Pharma, LLC is the labeler of record for Crysalo. 9 FDA label records share the active ingredient METHYL SALICYLATE, 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 Crysalo 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 Crysalo 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, MENTHOL?
Yes. 9 FDA drug label records list METHYL SALICYLATE, 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 Crysalo 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.