nail fungus treatment

nail fungus treatment is an FDA-registered drug product whose active ingredient is TOLNAFTATE. It is labelled by Guangzhou Liyan Cosmetics Technology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87770-003, application M005, label effective 20260612. It is one of 53 FDA drug label records sharing the active ingredient TOLNAFTATE. 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 TOLNAFTATE are most often described in connection with: treatment nail, fungusand associated, symptoms includ-ing, discoloration thickening, splitting crumbling. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For the treatment of nail fungusand associated symptoms includ-ing discoloration,thickening,splitting.crumbling.and brittleness

Apply the product twice a day, inthe morning and at night, or asdirected by a doctor. Before firstuse,soak the affected nail in warmwater to soften it. Gently file the nailsurface to remove debris and helpthe product penetrate, beingcautious not to harm the nail bed.For best results,file the nail surfaceonce weekly. Use the built-in brushapplicator to apply a thin layer ofthe solution evenly over the entireaffected nail, and if possible, underthe tip of the nail. Continue regularuse until the infection has clearedand healthy nail has grown back.Visible improvement may be seenwith continued use.

Do not use on children under 2years of age unless directed by adoctor.

FDA lists 53 drug label records with TOLNAFTATE 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 nail fungus treatment used for?
Uses For the treatment of nail fungusand associated symptoms includ-ing discoloration,thickening,splitting.crumbling.and brittleness

Who makes nail fungus treatment?
Guangzhou Liyan Cosmetics Technology Co., Ltd. is the labeler of record for nail fungus treatment. 53 FDA label records share the active ingredient TOLNAFTATE, 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 nail fungus treatment 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 nail fungus treatment 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 TOLNAFTATE?
Yes. 53 FDA drug label records list TOLNAFTATE 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 nail fungus treatment 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.