QQE Fungal Nail Treatment

TOLNAFTATE 1% TOPICAL HUMAN OTC DRUG

QQE Fungal Nail Treatment is an FDA drug label for the active ingredient TOLNAFTATE 1% manufactured by Guangzhou Huixue Biotechnology 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 20260505.

Generic name
TOLNAFTATE 1%
Manufacturer
Guangzhou Huixue Biotechnology Co., Ltd.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87204-175
Application
M005
Label effective
20260505

About this product

QQE Fungal Nail Treatment is an FDA-registered drug product whose active ingredient is TOLNAFTATE 1%. It is labelled by Guangzhou Huixue Biotechnology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87204-175, application M005, label effective 20260505. It is one of 39 FDA drug label records sharing the active ingredient TOLNAFTATE 1%. 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% are most often described in connection with: athlete foot, treatment nail, associated symptoms, including discoloration, thickening splitting, brittleness cures, tinea pedis, corporis relieves. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Tolnaftate 1%

Indications & Usage

For the treatment of nail fungus and associated symptoms, including discoloration, thickening, splitting, crumbling, and brittleness. 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

Use 2-3 times per week or as needed.,(5ml-10ml)each time.15 weeks supply

Warnings

For external use only. Do not use on children under 2 years of age unless directed by a doctor. When using this product, avoid contact with the eyes. Stop use and ask a doctor if irritation occurs or if there is no improvement within 4 weeks. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

More products with the same ingredient

TOLNAFTATE 1%

Anytalk FUNGAL NAIL TREATMENT

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BeamBalm ANTIFUNGAL FOOT CARE

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BeamBalm ANTIFUNGAL NAIL Liquid

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DERMFREE FUNGI NAIL

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FIobow FUNGAL NAIL TREATMENT

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FUNGAL NAIL NIGHTTIME RENEWAL PATCHES

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HEALMUSZ FOOT ODOR PROBIOTIC

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How products containing TOLNAFTATE 1% compare

FDA lists 39 drug label records with TOLNAFTATE 1% 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 24
— — Wenzhou Yuyuan Pharmaceutical Co., Ltd. 4
— — Beautivity LLC 3
— — 100 KARMA INC 2
— — Guangzhou Huixue Biotechnology Co., Ltd. 2

Frequently asked questions

What is QQE Fungal Nail Treatment used for?
For the treatment of nail fungus and associated symptoms, including discoloration, thickening, splitting, crumbling, and brittleness. 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 QQE Fungal Nail Treatment?
Guangzhou Huixue Biotechnology Co., Ltd. is the labeler of record for QQE Fungal Nail Treatment. 39 FDA label records share the active ingredient TOLNAFTATE 1%, 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 QQE 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 QQE 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%?
Yes. 39 FDA drug label records list TOLNAFTATE 1% 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 QQE 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.