DrAny NAIL FUNGUS TREATMENT

DrAny NAIL FUNGUS TREATMENT is an FDA-registered drug product whose active ingredient is UNDECYLENIC ACID, TOLNAFTATE. It is labelled by Hong Kong Juxin Negosyo Kag Komersyo Co., Limited taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87865-001, application M005, label effective 20260826. It is one of 3 FDA drug label records sharing the active ingredient UNDECYLENIC ACID, 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 UNDECYLENIC ACID, TOLNAFTATE are most often described in connection with: effective treatment, nail fungus, ssociated symptoms, including discoloration, thickening splitting. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For the effective treatment of nail fungus and ssociated symptoms, including discoloration, thickening, splitting, and crumbling.

Directions Directions • Clean and soak the toes (or fingers) in warm water, then pat dry. • Apply a thin layer over affected nails and surrounding skin. • Use twice daily (morning and evening).

Warnings Warnings For external use only. Do not use On children under 2 years of age unless directed by a doctor. When using this product Avoid contact with eyes.

FDA lists 3 drug label records with UNDECYLENIC ACID, 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 DrAny NAIL FUNGUS TREATMENT used for?
Uses For the effective treatment of nail fungus and ssociated symptoms, including discoloration, thickening, splitting, and crumbling.

Who makes DrAny NAIL FUNGUS TREATMENT?
Hong Kong Juxin Negosyo Kag Komersyo Co., Limited is the labeler of record for DrAny NAIL FUNGUS TREATMENT. 3 FDA label records share the active ingredient UNDECYLENIC ACID, 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 DrAny 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 DrAny 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 UNDECYLENIC ACID, TOLNAFTATE?
Yes. 3 FDA drug label records list UNDECYLENIC ACID, 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 DrAny 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.