Foot Choice-Nail Fungal Pen

Foot Choice-Nail Fungal Pen is an FDA-registered drug product whose active ingredient is UNDECYLENIC ACID. It is labelled by Foot Choice LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87830-001, application M005, label effective 20260717. It is one of 24 FDA drug label records sharing the active ingredient UNDECYLENIC ACID. 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 are most often described in connection with: effective treatment, nail fungus, 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 effective treatment of nail fungus, discoloration, thickening, splitting, crumbling, and brittleness.

Directions Apply the product twice a day, in the morning and at night. For initial use, soak the affected nail in warm water to soften it. Gently file the nail to make it thinner and remove dirt, being cautious not to harm the nail bed. For best results, file nails every 2–3 days. Use the Nail Repair Pen Brush to apply the solution to the affected areas. Visible results will be seen in as little as 7 days. Continue regular usage to prevent fungus regrowth.

Warnings For external use only.

FDA lists 24 drug label records with UNDECYLENIC ACID 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 Foot Choice-Nail Fungal Pen used for?
Uses For the effective treatment of nail fungus, discoloration, thickening, splitting, crumbling, and brittleness.

Who makes Foot Choice-Nail Fungal Pen?
Foot Choice LLC is the labeler of record for Foot Choice-Nail Fungal Pen. 24 FDA label records share the active ingredient UNDECYLENIC ACID, 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 Foot Choice-Nail Fungal Pen 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 Foot Choice-Nail Fungal Pen 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?
Yes. 24 FDA drug label records list UNDECYLENIC ACID 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 Foot Choice-Nail Fungal Pen 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.