Label: MENTHOL- maximum strength medicated foot powder powder

  • 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 irritation on the foot

  • ​Warnings

    ​For external use only.

    When using this product

    • avoid contact with eyes

    Stop and consult 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.

    In case of accidental ingestion, 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, eucalytus oil, gum acacia, peppermint oil, sodium bicarbonate, talc

  • ​Questions?

    Call 1-866-964-0939

  • Principal Display Panel

    Harmon

    FACEVALUES

    MAXIMUM STRENGTH

    Medicated

    Foot Powder

    Menthol 1%

    Triple Relief Formula

    • Absorbs Moisture
    • Relieves Itching
    • Controls Foot Odor

    NET WT 10 OZ (283 g)

    Harmon Medicated Foot PowderCV.jpg

  • INGREDIENTS AND APPEARANCE
    MENTHOL 
    maximum strength medicated foot powder powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63940-014
    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
    ACACIA (UNII: 5C5403N26O)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    TALC (UNII: 7SEV7J4R1U)  
    BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63940-014-10283 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/18/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/01/2012
    Labeler - Harmon Store Inc. (804085293)
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