Label: TOLNAFTATE- toe area treatment liquid
- NDC Code(s): 69842-274-01
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 2024
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- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
Read all warnings and directions. Use only as directed.
- 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 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 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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INGREDIENTS AND APPEARANCE
TOLNAFTATE
toe area treatment liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-274 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 0.3 g in 30 mL Inactive Ingredients Ingredient Name Strength PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) TOCOPHEROL (UNII: R0ZB2556P8) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-274-01 30 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 02/01/2021 05/30/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 02/01/2021 05/30/2025 Labeler - CVS Pharmacy (062312574)