Label: LOTRIMIN DAILY SWEAT AND ODOR CONTROL- topical starch powder

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated September 14, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Topical starch 83.7%

  • PURPOSE

    Purpose

    Skin Protectant

  • Use

    Use

    temporarily protects and helps relieve minor skin irritation

  • WARNINGS

    Warnings

    For external use only

    Do not use on broken skin.

    When using this product

    • Do not get into eyes

    • Keep away from face and mouth to avoid breathing it

    Stop use and ask a doctor if

    • Condition worsens
    • Symptoms last more than 7 days or clear up and occur again within a few days

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

  • Directions

    Directions

    Apply as needed

  • INACTIVE INGREDIENT

    Inactive ingredients

    benzethonium chloride,camphor,eucalyptus globulus leaf oil, fragrance, kaolin,lemon oil, zinc oxide

  • Questions

    Questions? 1-866-360-3266

  • Package display

    LOTRIMIN

    TOPICAL STARCH SKIN PROTECTANT

    medicated foot powder

    DAILY SWEAT

    & ODOR CONTROL

    6 odor-fighting

    ingredients to control odor

    • super sweat absorbent powder
    • relieves irritation
    • talc-free

    NET WT 177 G (6.25 OZ)

    Lotrimin Sweat and Odor Powder 0012 Front

    Lotrimin Sweat and Odor Powder 0012 Back

  • INGREDIENTS AND APPEARANCE
    LOTRIMIN DAILY SWEAT AND ODOR CONTROL 
    topical starch powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-0012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    STARCH, CORN (UNII: O8232NY3SJ) (STARCH, CORN - UNII:O8232NY3SJ) STARCH, CORN837 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    LEMON OIL (UNII: I9GRO824LL)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    KAOLIN (UNII: 24H4NWX5CO)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11523-0012-1177 g in 1 BOTTLE; Type 0: Not a Combination Product02/17/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34702/17/2020
    Labeler - Bayer HealthCare LLC. (112117283)
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