MiratiFul Nail Fungus Treatment

TOLNAFTATE TOPICAL HUMAN OTC DRUG

MiratiFul Nail Fungus Treatment is an FDA drug label for the active ingredient TOLNAFTATE manufactured by Texas MiratiFul Enterprises 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
Texas MiratiFul Enterprises Inc.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87885-001
Application
M005
Label effective
20260803

About this product

MiratiFul Nail Fungus Treatment is an FDA-registered drug product whose active ingredient is TOLNAFTATE. It is labelled by Texas MiratiFul Enterprises Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87885-001, 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: effective treatment, athlete foot, jock itch, relief infected, against bacteria. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Purpose Tolnaftate 1% Antifungal

Indications & Usage

Uses Effective treatment of athlete’s foot, jock itch, and ringworm. Not for the relief of infected fingernails and toenails or effective against bacteria or viruses.

Dosage & Administration

Directions ▪ Clean or 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 athelete’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; for jock itch, use daily for 2 weeks. If condition persists longer, consult a doctor. This product is not effective on the scalp or nails.

Warnings

Warnings ▪ For external use only. ▪ Avoid contact with the eyes. ▪ Do not use on children under 2 years of age unless directed by a doctor. ▪ Keep this and all drugs out of the reach of children. ▪ If treating athlete’s foot and ringworm: If irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor. ▪ If treating jock itch: If irritation occurs or if there is no improvement within 2 weeks, discontinue use and consult a doctor. ▪ If swallowed, get medical help or contact a Poison Control Center right away.

More products with the same ingredient

TOLNAFTATE

ACTIV-CHARCOAL ANTIFUNGAL

HONG KONG UNORDERED TRADING CO., LIMITED View label

ANTIFUNGAL BODY WASH

Guangzhou ChuanMa International Trading Co.,Ltd. View label

Aftate Athlete Foot Cream

Sabel Med LLC View label

Antifungal Liquid

Target Corporation View label

Antifungal Liquid

AmerisourceBergen Drug Corporation View label

Antifungal Liquid

Family Dollar Services, Inc View label

Antifungal Liquid

Walgreens Company View label

Athletes Foot

Rugby Laboratories View label

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 MiratiFul Nail Fungus Treatment used for?
Uses Effective treatment of athlete’s foot, jock itch, and ringworm. Not for the relief of infected fingernails and toenails or effective against bacteria or viruses.

Who makes MiratiFul Nail Fungus Treatment?
Texas MiratiFul Enterprises Inc. is the labeler of record for MiratiFul Nail Fungus Treatment. 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 MiratiFul Nail Fungus 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 MiratiFul Nail Fungus 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?
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 MiratiFul Nail Fungus 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.