Label: LIQUID ANTIFUNGAL TREATMENT- tolnaftate liquid
- NDC Code(s): 72446-012-01
- Packager: Hudson Health LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated April 1, 2024
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- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- wash the affected area and dry thoroughly.
- apply a thin layer of the product over 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.
- this product is not effective on the scalp or nails.
- Other information
- Inactive ingredient
- Questions?
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INGREDIENTS AND APPEARANCE
LIQUID ANTIFUNGAL TREATMENT
tolnaftate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72446-012 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 ACETONE (UNII: 1364PS73AF) WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72446-012-01 1 in 1 CARTON 03/29/2024 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 03/29/2024 Labeler - Hudson Health LLC (081276171)