OSIMOON Fungal Nail Treatment
OSIMOON Fungal Nail Treatment is an FDA drug label for the active ingredient FUNGAL NAIL TREATMENT manufactured by Guangzhou Jingliang Cosmetics Co., Ltd. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260414.
- Generic name
- FUNGAL NAIL TREATMENT
- Manufacturer
- Guangzhou Jingliang Cosmetics Co., Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87408-014
- Application
- M005
- Label effective
- 20260414
About this product
OSIMOON 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 87408-014, application M005, label effective 20260414. 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.
What it is used for
Across FDA labelling, products containing FUNGAL NAIL TREATMENT are most often described in connection with: treat damaged, cracked discolored. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses To treat damaged, cracked, or discolored nails.
Dosage & Administration
Directions ■ Soak your feet and hands in warm water to soften your ill toenails or fingernails. ■ Use the nail file to polish the nails, make them thin visibly, then scrap the dirt on the nails. ■ Brush liquid on infected nails and allow to absorb and dry. Apply two more layers of liquid, ensuring liquid is fully absorbed before each new stroke. ■ For best results, use Toenail Fungus Treatment two or three times a day. ■ Continue to use daily until fungus infection has been completely healed.
Warnings
Warnings • For external use only.
More products with the same ingredient
FUNGAL NAIL TREATMENTHow products containing FUNGAL NAIL TREATMENT compare
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.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Guangzhou Jingliang Cosmetics Co., Ltd. | 2 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is OSIMOON Fungal Nail Treatment used for?
Uses To treat damaged, cracked, or discolored nails.
Who makes OSIMOON Fungal Nail Treatment?
Guangzhou Jingliang Cosmetics Co., Ltd. is the labeler of record for OSIMOON 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 OSIMOON 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 OSIMOON 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 OSIMOON 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.