Label: MAXIMUM STRENGTH 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

    Temporary relief of pain and itch associated with:

    • minor cuts
    • sunburn
    • insect bites
    • scrapes
    • minor burns
    • minor skin irritations
  • Warning

    • For external use only
    • Avoid contact with eyes

    Stop use and ask a doctor if

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

    Remove seal beneath cap before first use. Do not use if seal is broken

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

    For best results, dry skin throughly before applying

  • Inactive ingredients

    Zea Mays (Corn) Starch, Tricalcium Phosphate,  Sodium Bicarbonate, Benzethonium Chloride, Eucalyptus Oil, Peppermint Oil

  • PRINCIPAL DISPLAY PANEL

    NDC 42669-283-01

    CVS HEALTH Compared to the active ingredient in Maximum Strength Gold bond Medicated Foot Powder*

    MAXIMUM STRENGTH Medicated Foot Powder WITH CORNSTARCG

    • Triple Relief: controls odor, absorbs moisture & relieves itc
    • Soothing formula
    • Clinically tested
    • Talc free

    NET WT 10 OZ (283 g)

    Label

  • INGREDIENTS AND APPEARANCE
    MAXIMUM STRENGTH MEDICATED FOOT POWDER 
    menthol powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42669-283
    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
    STARCH, CORN (UNII: O8232NY3SJ)  
    TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42669-283-01283 g in 1 BOTTLE; Type 0: Not a Combination Product01/30/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/30/2018
    Labeler - Davion, Inc (174542928)
    Registrant - Davion, Inc (079536689)
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