Dryello Tolnaftate 1% Antifungal

Dryello Tolnaftate 1% Antifungal is an FDA-registered drug product whose active ingredient is TOLNAFTATE. It is labelled by ProPedix, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85565-008, application M005, label effective 20260810. 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.

Across FDA labelling, products containing TOLNAFTATE are most often described in connection with: athlete foot, tinea pedis, relieves itching, burning cracking, scaling prevents. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Cures most Athlete's Foot (tinea pedis) Relieves itching, burning, cracking, and scaling Prevents recurrence of most Athlete's foot with daily use

Directions Wash feet and dry thoroughly. Apply a thin layer of the product to the affected area twice daily (morning and night). Supervise children in the use of this product. Pay special attention to spaces between toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.

Warnings Do not use on children under 2 years of age unless directed by a doctor. For external use only. Avoid contact with eyes. When using this product If irritation occurs, discontinue use and consult a doctor Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

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.

What is Dryello Tolnaftate 1% Antifungal used for?
Uses Cures most Athlete's Foot (tinea pedis) Relieves itching, burning, cracking, and scaling Prevents recurrence of most Athlete's foot with daily use

Who makes Dryello Tolnaftate 1% Antifungal?
ProPedix, Inc. is the labeler of record for Dryello Tolnaftate 1% Antifungal. 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 Dryello Tolnaftate 1% Antifungal 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 Dryello Tolnaftate 1% Antifungal 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 Dryello Tolnaftate 1% Antifungal 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.