Tolnaftate Antifungal Powder
FDA Label NDC 73469-0619

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Scholl's Wellness Company Llc for the product Tolnaftate Antifungal Powder (NDC 73469-0619). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, directios, other information, inactive ingredients, questions ?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Tolnaftate 1%

Purpose

Antifungal

Use

  • Clinically proven to prevent most athlete's foot (tinea pedis) with daily use

Warnings

For External use only

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

Other Information

Store between 20° to 25°C (68° to 77°F)

Inactive Ingredients

Chloroxylenol, Fragrance, Kaolin, Sodium Bicarbonate, Tricalcium Phosphate, Zea Mays (Corn) Starch, Zinc Oxide

Questions ?

1-866-360-3226

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