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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Bayer Healthcare Llc. for the product Lotrimin Daily Prevention (NDC 11523-0011). 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 other, otc - active ingredient, otc - purpose, use, warnings, otc - do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Active ingredient
Tolnaftate 1%
Purpose
Antifungal
Use
• clinically proven to prevent most athlete' s foot with daily use
Warnings
For external use only
Do not use on children under 2 years of age unless directed by a doctor
When using this product avoid contact with the eyes
Stop use and ask a doctor if irritation occurs
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• to prevent athlete's foot, wash the feet and dry 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 socks at least
once daily.
Other information
store between 20° to 25°C (68°– 77°F)
Inactive ingredients
benzethonium chloride;corn starch, kaolin;sodium bicarbonate
Questions? 1-866-360-3266
LOTRIMIN® AF
TOLNAFTATE ANTIFUNGAL
medicated foot powder
DAILY
PREVENTION
clinically proven to
prevent most
athlete's foot
NET WT 90g (3 OZ)
* Please review the disclaimer below.