Active Ingredient
Tolnaftate 1%
The following Structured Product Label (SPL) was submitted to the FDA by Premier Brands Of America Inc. for the product Foot Odor Control Powder (NDC 56104-252). 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, uses, warnings, flammable:, when using this product, stop use and ask a doctor if, do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Tolnaftate 1%
Antifungal
For external use only.
Keep away from heat, sparks and open flame. Contents under pressure. Do not puncture or incinerate. Do not store above 120°F. Intentional misuse by deliberately concentrating and inhaling the contents cans be harmful or fatal.
on children under 2 years of age unless directed by a doctor.
If swallowed, get medical help or contact a Poison Control Center right away.
store between 20° and 30°C (68° and 86°F)
disteardimonium hectorite, fragrance, isobutane, isopropyl myristate, SD alcohol 40-B, sodium bicarbonate
Call 888-964-0939
Odor Control
Foot
Powder
Spray
TOLNAFTATE 1%/
ANTIFUNGAL
REDUCES ODOR
& Reduces Foot Odor
Relieves Itching, Cracking & Burning
Talc-Free
NET WT 4 OZ (113g)
* Please review the disclaimer below.