Label: MAXIMUM STRENGTH MEDICATED FOOT POWDER- medicated foot powder powder

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

Drug Label Information

Updated December 18, 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 cuts

    -scrapes

    -sunburn

    -insect bites

    -prickly heat

    -rashes

    -minor burns

    -minor skin irritation

    -dries the oozing of poison ivy, oak and sumac.

  • ​Warnings

    ​For external use only.

    ​When using this product

    • avoid contact with eyes. Not for genital area

    Stop and consult a doctor if

    • conditions worsens
    • redness, irritation, swelling or pain persist or increases
    • symptoms do not get better within 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 (1-800-222-1222) right away.

  • ​Directions

    • adults and children 2 years of age and over: apply freely up to 3 or 4 times daily
    • children under 2 years: consult a physician
    • For best results, dry skin thoroughly before use.
  • ​Inactive ingredients

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

  • Maximum Strength Medicated Foot Powder

    label

  • INGREDIENTS AND APPEARANCE
    MAXIMUM STRENGTH MEDICATED FOOT POWDER 
    medicated foot powder powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-795
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.1 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    ZEA MAYS WHOLE (UNII: 1G5HNE09V8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-795-01283 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01709/01/2020
    Labeler - Walmart Stores Inc (051957769)
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