Label: WALGREENS MEDICATED FOOT POWDER- menthol powder

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 28, 2024

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  • Active Ingredient

    Menthol 1.0%

  • Purpose

    External Analgesic

  • Uses

    For the temporary relief of pain and itch associate with minor skin irritations on the foot

  • Warning

    • For external use only

    When using this product

    • avoid contact with eyes

    Stop use and ask a doctor if

    • condition worsens
    • symptoms persists for more than 7 days or clear up and occur again within a few days

    Keep out of reach of children

    In case of accidental ingestion, get medical help or contact a poison control center right away.

  • Directions

    • adults and children 2 years and older - apply freely upto 3 or 4 times daily
    • children under 2 years - ask a doctor

      Thoroughly wash and dry feet, sprinkle powder liberally over feet, between toes and on bottom of feet and in shoes
  • Inactive ingredients

    Talc, Sodium Bicarbonate, Acacia, Benzethonium Chloride, Eucalyptus Oil, Peppermint Oil

  • Principal Display Panel

    NDC 42669-100-10

    WALGREENS FOOT POWDER

    Compare to Gold Bond Medicated Foot Powder active ingredient

    Foot Powder

    MENTHOL 1.0%/ EXTERNAL ANALGESIC

    MAXIMUM STRENGTH

    MEDICATED

    Absorbs Moisture
    Helps control foot odor

    NET WT 10 OZ (283 g)

    Label

  • INGREDIENTS AND APPEARANCE
    WALGREENS MEDICATED FOOT POWDER 
    menthol powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42669-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    TALC (UNII: 7SEV7J4R1U)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    ACACIA (UNII: 5C5403N26O)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42669-100-10283 g in 1 BOTTLE; Type 0: Not a Combination Product06/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01706/01/2018
    Labeler - Davion, Inc (174542928)
    Registrant - Davion, Inc (079536689)
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