Tolnaftate Antifungal Powder 1 g/100g
Tolnaftate · POWDER · SCHOLL'S WELLNESS COMPANY LLC
Tolnaftate Antifungal Powder is a powder containing tolnaftate at 1 g/100g, taken topical. Manufactured by SCHOLL'S WELLNESS COMPANY LLC.
Key Facts
- Brand Name
- Tolnaftate Antifungal Powder
- Generic Name
- Tolnaftate
- NDC Code (Product)
73469-0619- Manufacturer
- SCHOLL'S WELLNESS COMPANY LLC
- Strength
- 1 g/100g
- Dosage Form
- POWDER
- Route
- TOPICAL
- Marketing Status
- Application #
- M005
- Marketing Start
- 11/26/2025
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
Use Clinically proven to prevent most athlete's foot (tinea pedis) with daily use
Dosage & Administration
Directios to prevent athlete's foot, wash and dry feet thoroughly apply a thin layer of the product on 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
Warnings
Warnings For External use only
Frequently Asked Questions
What is Tolnaftate Antifungal Powder used for?
Tolnaftate Antifungal Powder contains Tolnaftate. It is a powder taken topical. Consult your doctor for specific uses.
Is Tolnaftate Antifungal Powder a controlled substance?
Tolnaftate Antifungal Powder is not classified as a controlled substance by the DEA.
What is the generic name for Tolnaftate Antifungal Powder?
The generic name for Tolnaftate Antifungal Powder is Tolnaftate. There are 11 other brand versions of Tolnaftate.
What is the NDC code for Tolnaftate Antifungal Powder 1 g/100g?
The NDC (National Drug Code) for Tolnaftate Antifungal Powder 1 g/100g is 73469-0619, listed by SCHOLL'S WELLNESS COMPANY LLC.
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)