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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Bayer Healthcare Llc. for the product Tinactin (NDC 11523-0139). 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, active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Tolnaftate 1%
Antifungal
For external use only
Flammable: Do not use near heat, flame, or while smoking
Do not use on children under 2 years of age unless directed by a doctor.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
store between 20° to 25°C (68° to 77°F)
butylated hydroxytoluene, hydroxypropyl cellulose, isobutane,kaolin, magnesium stearate, PPG-12-buteth-16, SD alcohol 40-B (9% w/w), zea mays (corn) starch
1-866-360-3266
TOUGH ACTIN' ®
Tinactin ®
tolnaftate ANTIFUNGAL
Cures and prevents
most athlete's foot
Relieves
POWDER SPRAY
goes on dry
talc free
NET WT 133g (4.6 oz)
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