TINEACIDE
TINEACIDE is an FDA drug label for the active ingredient TOLNAFTATE manufactured by Blaine Labs Inc. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231221.
Generic: TOLNAFTATE
Manufacturer: Blaine Labs Inc.
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 63347-511
Application: M005
Effective: 20231221
Active Ingredients: Active Ingredients Drug facts Active Ingredient TOLNAFTATE 1%
Indications & Usage
Indications Indications Cures most athlete's foot (tinea pedis). Cures most jock itch (tinea cruris) and ring worm (tinea corporis). Relieves itching, cracking, burning, and scaling which accompany these conditions. Prevents most athlete's foot (tinea pedis) with daily use.
Dosage & Administration
Directions Directions Wash the affected ares with soap and water and dry thoroughly. Apply a thin layer over affected area twice daily (morning and night) or as directed by a physician. Supervise children in the use of this product. For athlete's foot pay special attention to spaces between the toes, wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. For athlete's foot and ringworm, use daily for 4 weeks. For jock itch, use daily for 2 weeks. If condition persists longer, consult a physician. wash hands after each use.
Contraindications
Not available.
Warnings
Warnings Warnings Do not use on children under 2 years of age unless directed by a physician in or near mouth or eyes for vaginal yeast infections For external use only
Adverse Reactions
Not available.
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