Active Ingredient
Tolnaftate 1%
The following Structured Product Label (SPL) was submitted to the FDA by Hudson Health Llc for the product Liquid Antifungal Treatment (NDC 72446-012). 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, do not use, when using this product, stop use and consult a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Tolnaftate 1%
Antifungal
for the treatment of athlete’s foot (tinea pedis) and ringworm (tinea corporis)
for effective relief of itching, scaling, cracking, burning and redness.
For external use only.
keep away from fire or flame.
on children under 2 years of age unless directed by a doctor.
avoid contact with the eyes.
If swallowed, get medical help, or contact a Poison Control Center right away.
Acetone, Water, Propylene Glycol, Tocopherol Acetate.
Call 1-866-964-0939
Comfort zone
liquid antifungal treatment
with vitamin e to moisturize
TOLNAFTATE 1%/ANTIFUNGAL
Maxiumum Strength
Brush- On Applicator
SHAKE WELL BEFORE USE
1 FL. OZ. (30 mL)
* Please review the disclaimer below.