Uauko Fungal Nail Treatment

Uauko Fungal Nail Treatment is an FDA-registered drug product whose active ingredient is FUNGAL NAIL TREATMENT. It is labelled by Guangzhou Jingliang Cosmetics Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87408-018, application M005, label effective 20260502. It is one of 2 FDA drug label records sharing the active ingredient FUNGAL NAIL TREATMENT. 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 FUNGAL NAIL TREATMENT are most often described in connection with: hinder fungal, bacterial growth, reduce itching, cleanse skin. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Hinder fungal and bacterial growth, reduce itching, cleanse skin tissue.

Directions ■ Before using it, clean the affected area with soap and soak the nail with warm water to soften it. ■ For toe fungus, scrape off the dirt on the nail, and gently file the thickened part of the fungal nail with a nail file until it's flat. (be careful not to hurt the nail bed) You can use a nail file every 2-3 days to polish the surface of the affected area. Apply the liquid with a thin layer over the affected area, underneath nail tips, and around the cuticle area. ■ For athlete's foot, pay special attention to spaces between toes. ■ Use it twice in the morning and evening for at least 6 weeks to see the effect. And if you want complete improvement, we recommend using it for 3-6 months or longer. ■ You can use this product preventively for fungus in hot and humid conditions.

Warnings • For external use only. • When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water. • Stop use and ask/ consult a doctor/ physician/ health care practitioner/ health care provider/ health care professional if irritation or symptoms worsen or last for more than 4 weeks. • Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away.

FDA lists 2 drug label records with FUNGAL NAIL TREATMENT 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 Uauko Fungal Nail Treatment used for?
Uses Hinder fungal and bacterial growth, reduce itching, cleanse skin tissue.

Who makes Uauko Fungal Nail Treatment?
Guangzhou Jingliang Cosmetics Co., Ltd. is the labeler of record for Uauko Fungal Nail Treatment. 2 FDA label records share the active ingredient FUNGAL NAIL TREATMENT, 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 Uauko Fungal Nail 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 Uauko Fungal Nail 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 FUNGAL NAIL TREATMENT?
Yes. 2 FDA drug label records list FUNGAL NAIL TREATMENT 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 Uauko Fungal Nail 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.