Active Ingredient
Tolnaftate 1%
The following Structured Product Label (SPL) was submitted to the FDA by Premier Brands Of America Inc for the product Antifungal Liquid (NDC 56104-902). 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, do not use, when using this product, stop use and consult a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Tolnaftate 1%
Antifungal
proven clinically effective in the treatment of most athlete's foot (tinea pedis) and ringworm (tinea corporis)
prevents the recurrence of most athlete's foot with daily use
for effective relief of itching, burning, cracking, redness and scaling
For external use only.
on children under 2 years of age unless directed by a doctor.
avoid contact with the eyes.
If accidental ingestion occurs, get medical help or contact a Poison Control Center right away.
WATER, GLYCERIN, SCLEROTIUM GUM, PHENOXYETHANOL, DISODIUM EDTA, ETHYLHEXYLGLYCERIN, XANTHAN GUM
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premier
solutions
Maximum Strength
ANTIFUNGAL
LIQUID
TOLNAFTATE 1%/
ANTIFUNGAL
PROVEN CLINICALLY
EFFECTIVE IN THE
TREATMENT OF FUNGUS
ON FINGERS, TOES AND
SKIN AROUND NAILS
Prevents the recurrence
of most athlete's foot with
daily use
Relieves itching,
scaling & burning
With moisturizing
ingredients
SHAKE WELL
BEFORE USE
1 FL. OZ. (30 mL)
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