FIobow FUNGAL NAIL TREATMENT

TOLNAFTATE 1% FUNGAL NAIL TREATMENT TOPICAL HUMAN OTC DRUG

FIobow FUNGAL NAIL TREATMENT is an FDA drug label for the active ingredient TOLNAFTATE 1% FUNGAL NAIL TREATMENT manufactured by Jiangxi Yudexi Pharmaceutical 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 20260623.

Generic name
TOLNAFTATE 1% FUNGAL NAIL TREATMENT
Manufacturer
Jiangxi Yudexi Pharmaceutical Co., LTD
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
85248-095
Application
M005
Label effective
20260623

About this product

FIobow FUNGAL NAIL TREATMENT is an FDA-registered drug product whose active ingredient is TOLNAFTATE 1% FUNGAL NAIL TREATMENT. It is labelled by Jiangxi Yudexi Pharmaceutical Co., LTD taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85248-095, application M005, label effective 20260623. It is one of 2 FDA drug label records sharing the active ingredient TOLNAFTATE 1% 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 TOLNAFTATE 1% FUNGAL NAIL TREATMENT are most often described in connection with: athlete foot, tinea pedis, corporis relieves, itching scaling, cracking burning, redness soreness, discomfort helps. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Tolnaftate 1%

Indications & Usage

Use Cures most Athlete's Foot (Tinea Pedis)and Ringworm (Tinea Corporis). Relieves itching, scaling, cracking, burning,redness, soreness, irritation and discomfort. Helps prevent most athlete's foot (dermatophytosis) with daily use.

Dosage & Administration

Directions Directions For athlete's foot and ringworm: use daily for 4 weeks. Clean the affected area and dry thoroughly. Apply a thin layer of the product over affected area twice daily (morning and night) or as directed by a doctor. Supervise children in the use of this product. This product is not effective for the treatment of ringworm of the scalp or nails. For athlete's foot: pay special attention to spaces between the toes, wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. To prevent athlete's foot, apply once or twice daily(morning and/or night). Apply to skin around the nail and cuticle.

Warnings

Warnings For external use only.

More products with the same ingredient

TOLNAFTATE 1% FUNGAL NAIL TREATMENT

OURUI ONE FUNGAL NAIL TREATMENT

Jiangxi Yudexi Pharmaceutical Co., LTD View label

How products containing TOLNAFTATE 1% FUNGAL NAIL TREATMENT compare

FDA lists 2 drug label records with TOLNAFTATE 1% 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 formProductsManufacturerProducts
— — Jiangxi Yudexi Pharmaceutical Co., LTD 2
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Frequently asked questions

What is FIobow FUNGAL NAIL TREATMENT used for?
Use Cures most Athlete's Foot (Tinea Pedis)and Ringworm (Tinea Corporis). Relieves itching, scaling, cracking, burning,redness, soreness, irritation and discomfort. Helps prevent most athlete's foot (dermatophytosis) with daily use.

Who makes FIobow FUNGAL NAIL TREATMENT?
Jiangxi Yudexi Pharmaceutical Co., LTD is the labeler of record for FIobow FUNGAL NAIL TREATMENT. 2 FDA label records share the active ingredient TOLNAFTATE 1% 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 FIobow 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 FIobow 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 TOLNAFTATE 1% FUNGAL NAIL TREATMENT?
Yes. 2 FDA drug label records list TOLNAFTATE 1% 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 FIobow 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.