Label: MENTHOL- maximum strength medicated foot powder powder

  • NDC Code(s): 63941-558-10
  • Packager: VALU MERCHANDISERS, CO
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 12, 2024

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  • ​Active ingredient

    Menthol 1.0%

  • Purpose

    External analgesic

  • ​Use

    for the temporary relief of pain and itching associated with minor skin irritations

  • ​Warnings

    ​For external use only.

    When using this product

    • avoid contact with the eyes

    Stop use and ask a doctor if

    • conditions worsens
    • symptoms persists for 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

    • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
    • children under 2 years of age: consult a doctor
    • wash and dry feet thoroughly
    • sprinkle powder liberally on feet, between toes and on bottoms of feet
  • ​Inactive ingredients

    benzethonium chloride, eucalyptus oil, peppermint oil, sodium bicarbonate, tricalcium phosphate, zea mays (corn) starch

  • ​Questions?

    Call 1-866-964-0939

  • Principal Display Panel

    Best Choice

    MAXIMUM STRENGTH

    Medicated Foot Powder

    MENTHOL 1.0% / EXTERNAL ANALGESIC

    TALC-FREE

    • Absorbs Moisture
    • Relieves Itching
    • Helps Control Foot Odor

    NET WT 10 oz (283g)

    best choice

  • INGREDIENTS AND APPEARANCE
    MENTHOL 
    maximum strength medicated foot powder powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63941-558
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2.8 g  in 283 g
    Inactive Ingredients
    Ingredient NameStrength
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
    BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63941-558-10283 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/15/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01707/15/2019
    Labeler - VALU MERCHANDISERS, CO (868703513)
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