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

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated September 29, 2020

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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 not finalpart34809/01/2020
    Labeler - Walmart Stores Inc (051957769)
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