Fungi Nail Everyday Antifungal Powder

Fungi Nail Everyday Antifungal Powder is an FDA-registered drug product whose active ingredient is TOLNAFTATE. It is labelled by Kramer Laboratories taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 55505-234, application M005, label effective 20260701. 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: helps prevent, athlete foot. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use helps prevent most athlete's foot with daily use.

Directions ■ To prevent athlete's foot, wash and dry feet thoroughly ■ Shake can well and spray a thin layer of the product to the feet once or twice daily (morning and/or night) ■ Supervise children in the use of this product. ■ Pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily ■ In case of clogging, clean nozzle with pin.

Warnings For external use only.

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.

2 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

What is Fungi Nail Everyday Antifungal Powder used for?
Use helps prevent most athlete's foot with daily use.

Who makes Fungi Nail Everyday Antifungal Powder?
Kramer Laboratories is the labeler of record for Fungi Nail Everyday Antifungal Powder. 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 Fungi Nail Everyday Antifungal Powder 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 Fungi Nail Everyday Antifungal Powder 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 Fungi Nail Everyday Antifungal Powder been recalled?
2 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.