Label: LOTRIMIN DAILY PREVENT DEODORANT- tolnaftate aerosol, powder
- NDC Code(s): 11523-0136-1
- Packager: Bayer HealthCare LLC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 25, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- Use
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WARNINGS
Warnings
For external use only
Flammable: Do not use near heat, flame, or while smoking
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Directions
Directions
- to prevent athlete’s foot, wash the feet and dry thoroughly.
- shake can well and spray a thin layer of the product on the feet once or twice daily (morning and/or night).
- supervise children in the use of this product.
- pay special attention to spaces between the toes; wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.
- Other information
- INACTIVE INGREDIENT
- QUESTIONS
- Display can 160 grams
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INGREDIENTS AND APPEARANCE
LOTRIMIN DAILY PREVENT DEODORANT
tolnaftate aerosol, powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11523-0136 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 g Inactive Ingredients Ingredient Name Strength MAGNESIUM STEARATE (UNII: 70097M6I30) STARCH, CORN (UNII: O8232NY3SJ) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) ALCOHOL (UNII: 3K9958V90M) HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH) PPG-12-BUTETH-16 (UNII: 58CG7042J1) ISOBUTANE (UNII: BXR49TP611) KAOLIN (UNII: 24H4NWX5CO) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11523-0136-1 160 g in 1 CAN; Type 0: Not a Combination Product 03/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 03/01/2024 Labeler - Bayer HealthCare LLC. (112117283)