Label: MENTHOL- maximum strength medicated foot powder talc free powder

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

Drug Label Information

Updated December 11, 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

  • 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

    benzathonium Chloride, eucalyptus oil, peppermint oil, sodium bicarbonate, tricalcium phosphate, zea mays (corn) starch

  • Questions?

    Call - 1-888-423-0139

  • Principal Display Panel

    Top Care health

    MAXIMUM STRENGTH

    Medicated Foot Powder

    MENTHOL 1%

    EXTERNAL ANALGESIC

    TALC- FREE

    Triple-Action Formula

    • Absorbs Moisture
    • Relieves Itching
    • Helps Control Foot Odor

    NET WT 10 OZ (283g)

    Medicated Foot Powder Talc Free

  • INGREDIENTS AND APPEARANCE
    MENTHOL 
    maximum strength medicated foot powder talc free powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:36800-252
    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
    ZEA MAYS SUBSP. MAYS WHOLE (UNII: 1G5HNE09V8)  
    TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:36800-252-10283 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/10/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/10/2019
    Labeler - Topco Associates LLC (006935977)
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