Maximum Strength Antifungal Liquid

TOLNAFTATE TOPICAL HUMAN OTC DRUG

Maximum Strength Antifungal Liquid is an FDA drug label for the active ingredient TOLNAFTATE manufactured by Meijer Distribution Inc 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 20260803.

Generic name
TOLNAFTATE
Manufacturer
Meijer Distribution Inc
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
79481-0660
Application
M005
Label effective
20260803

About this product

Maximum Strength Antifungal Liquid is an FDA-registered drug product whose active ingredient is TOLNAFTATE. It is labelled by Meijer Distribution Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 79481-0660, application M005, label effective 20260803. It is one of 53 FDA drug label records sharing the active ingredient TOLNAFTATE. 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 are most often described in connection with: treament athlete, foot tinea, ring worm, effective relief, itching scaling, cracking burning. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

​Active ingredient Tolnaftate 1% w/w

Indications & Usage

Uses For the treament of athlete's foot (tinea pedis) and ring worm (tinea corporis). For effective relief of itching, scaling, cracking, burning, and redness.

Dosage & Administration

​Directions wash the affected area and dry thoroughly. apply a thin layer of the product over the affected area twice daily (morning and night) or as directed by a doctor. supervise children in the use of this product. for athlete's foot: pay special attention to spaces between toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. for athlete's foot and ringworm, use daily for 4 weeks. If condition persists longer, consult a doctor. this product is not effective on the scalp or nails.

Warnings

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 consult 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. Flammable Keep away from fire or flame.

More products with the same ingredient

TOLNAFTATE

ACTIV-CHARCOAL ANTIFUNGAL

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Aftate Athlete Foot Cream

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AmerisourceBergen Drug Corporation View label

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How products containing TOLNAFTATE compare

FDA lists 53 drug label records with TOLNAFTATE 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
— — Guangdong Aimu Biological Technology Co., Ltd 6
— — GUANGZHOU SAWEILAN IMPORT & EXPORT TRADING CO., LTD 4
— — Rida LLC 4
— — Clinical Therapeutic Solutions 3
— — Guangzhou ChuanMa International Trading Co.,Ltd. 2

Frequently asked questions

What is Maximum Strength Antifungal Liquid used for?
Uses For the treament of athlete's foot (tinea pedis) and ring worm (tinea corporis). For effective relief of itching, scaling, cracking, burning, and redness.

Who makes Maximum Strength Antifungal Liquid?
Meijer Distribution Inc is the labeler of record for Maximum Strength Antifungal Liquid. 53 FDA label records share the active ingredient TOLNAFTATE, 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 Maximum Strength Antifungal Liquid 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 Maximum Strength Antifungal Liquid 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?
Yes. 53 FDA drug label records list TOLNAFTATE 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 Maximum Strength Antifungal Liquid 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.