Aiilo NAIL FUNGUS TREATMENT

Aiilo NAIL FUNGUS TREATMENT is an FDA-registered drug product whose active ingredient is UNDECYLENIC ACID 25%. It is labelled by Guangzhou Huixue Biotechnology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87204-190, application M005, label effective 20260713. It is one of 31 FDA drug label records sharing the active ingredient UNDECYLENIC ACID 25%. 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 25% are most often described in connection with: including discoloration, thickening splitting, brittleness directions, product twice, affected nail, warm water, soften gently, make thinner. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

including discoloration, thickening, splitting, crumbling, and brittleness.Directions: 1 Apply the product twice a day, in the morning and at night 2. For initial use, soak the affected nail in warm water to soften it, Gently file the nail to make it thinner and remove debris, being cautious not to harm the nail bed, For best results file nails every 2-3 days 3. Hold the bottle at an angle and apply 2-3 drops of the solution evenly to the affected area 4 Visible improvement may be seen in as little as 7 days, Continue regular use to help prevent fungus regrowth.

FDA lists 31 drug label records with UNDECYLENIC ACID 25% 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 Aiilo NAIL FUNGUS TREATMENT used for?
including discoloration, thickening, splitting, crumbling, and brittleness.Directions: 1 Apply the product twice a day, in the morning and at night 2. For initial use, soak the affected nail in warm water to soften it, Gently file the nail to make it thinner and remove debris, being cautious not to harm the nail bed, For best results file nails every 2-3 days 3. Hold the bottle at an angle and …

Who makes Aiilo NAIL FUNGUS TREATMENT?
Guangzhou Huixue Biotechnology Co., Ltd. is the labeler of record for Aiilo NAIL FUNGUS TREATMENT. 31 FDA label records share the active ingredient UNDECYLENIC ACID 25%, 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 Aiilo 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 Aiilo 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 25%?
Yes. 31 FDA drug label records list UNDECYLENIC ACID 25% 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 Aiilo 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.