Label: ANTIFUNGAL LIQUID- tolnaftate liquid
- NDC Code(s): 82442-956-01
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 24, 2024
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- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- clean the affected area and dry thoroughly
- apply a thin layer of the product over the affected area twice daily (morning and night) or as directed by a doctor
- 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.
- if condition persists longer, consult a doctor
- to prevent athlete's foot: wash the feet and dry thoroughly; apply a thin layer of the product to the feet once or twice daily (morning and/or night)
- this product is not effective on the scalp or nails
- Other information
- Inactive ingredient
- Questions?
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Principal Display Panel
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, Burning
& Scaling
Built-in Brush for Easy
Application
With moisturizing Ingredients
SHAKE WELL BEFORE USE
NET 1 FL. OZ. (30 mL)
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INGREDIENTS AND APPEARANCE
ANTIFUNGAL LIQUID
tolnaftate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82442-956 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) XANTHAN GUM (UNII: TTV12P4NEE) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) EDETATE DISODIUM (UNII: 7FLD91C86K) PHENOXYETHANOL (UNII: HIE492ZZ3T) BETASIZOFIRAN (UNII: 2X51AD1X3T) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82442-956-01 1 in 1 CARTON 07/19/2024 1 30 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 07/19/2024 Labeler - Target Corporation (006961700)