Label: TOLNAFTATE- antifungal liquid spray aerosol, spray
- NDC Code(s): 69256-034-53
- Packager: Harris Teeter, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 29, 2024
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- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- wash affected area and dry thoroughly
- shake can well and spray a thin layer over affected area twice daily (morning and night)
- 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
- use daily for 4 weeks
- if conditions persist, consult a doctor
- to prevent athlete's foot, apply once or twice daily (morning and/or night)
- this product is not effective on the scalp or nails
- Other information
- Inactive ingredients
- Questions?
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INGREDIENTS AND APPEARANCE
TOLNAFTATE
antifungal liquid spray aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69256-034 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE 1.5 g in 150 g Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) ISOBUTANE (UNII: BXR49TP611) PPG-12-BUTETH-16 (UNII: 58CG7042J1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69256-034-53 150 g in 1 CAN; Type 0: Not a Combination Product 12/21/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 12/21/2017 Labeler - Harris Teeter, LLC (048463103)