Active Ingredient
Tolnaftate 1%
The following Structured Product Label (SPL) was submitted to the FDA by Propedix, Inc. for the product Dryello Tolnaftate 1% Antifungal (NDC 85565-005). 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, when using this product, keep out of reach of children, directions, other, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Tolnaftate 1%
Antifungal
Do not use on children under 2 years of age unless directed by a doctor.
For external use only. Avoid contact with eyes.
If swallowed, get medical help or contact a Poison Control Center right away.
Store between 68° - 86°F (20° - 30°C)
Aluminum Hydroxide, Arrowroot Powder, Behenyl Behenate, C12-15 Alkyl Benzoate, Cyclopentasiloxane, Magnesium Aluminum Silicate, Magnesium Citrate, Magnesium Hydroxide, Magnesium Sulfate, Orange Peel Oil, Stearyl Alcohol, Tocopheryl Acetate.
1-800-452-7362 dryello.com
For Athlete's Foot
Treats + Prevents
New Silky Smooth Application
Dryello TM
TOLNAFTATE 1% ANTIFUNGAL
Vlinically Proven
Dermatologist Developed
Two Glide-On Sticks
Two 15g (0.53oz) NET WT Sticks
* Please review the disclaimer below.