Label: LOTRIMIN DAILY PREVENT DEODORANT- tolnaftate aerosol, powder

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated June 25, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active Ingredient

    (To Deliver)Tolnaftate 1%

  • PURPOSE

    Purpose

    Antifungal

  • Use

    Use

    clinically proven to prevent most athlete’s foot with daily use

  • WARNINGS

    Warnings

    For external use only

    Flammable: Do not use near heat, flame, or while smoking

    Do not use on children under 2 years of age unless directed by a doctor

    When using this product

    • avoid contact with the eyes
    • use only as directed. Intentional misuse by deliberately concentrating and inhaling contents can be harmful or fatal.
    • contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120ºF.

    Stop use and ask a doctor if irritation occurs.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • 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

    Other Information

    store between 20º to 25ºC (68º– 77ºF)

  • INACTIVE INGREDIENT

    Inactive Ingredients

    butylated hydroxytoluene, fragrance, hydroxypropyl cellulose, isobutane, kaolin, magnesium stearate, PPG-12-Buteth-16, SD alcohol 40B (9% w/w), zea mays (corn) starch

  • QUESTIONS

    Questions?1-866-360-3266 or visit us at www.lotrimin.com

  • Display can 160 grams

    PDP

  • INGREDIENTS AND APPEARANCE
    LOTRIMIN  DAILY PREVENT DEODORANT
    tolnaftate aerosol, powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-0136
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    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
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11523-0136-1160 g in 1 CAN; Type 0: Not a Combination Product03/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00503/01/2024
    Labeler - Bayer HealthCare LLC. (112117283)
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