Label: MEDICATED BODY POWDER- menthol powder

  • NDC Code(s): 79903-724-01, 79903-724-04
  • Packager: Walmart Stores Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 18, 2024

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  • Drug Facts Active Ingredients

    Menthol 0.15 %

  • Purpose

    External Analgesic

  • Uses

    for the temporary relief of the pain and itch associated with

    • minor cuts
    • scrapes
    • sunburn
    • insect bites
    • prickly heat
    • rashes
    • minor burns
    • minor skin irritations
    • dries the oozing of poison ivy, oak and sumac.

  • Warnings

    For external use only

  • When usin this product

    Avoid contact with eyes. Not for genital area.

  • Stop use and ask a doctor if

    • condition 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

    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

    acacia seyl gum, eucalyptol, methyl salicylate, salicylic acid, sodium bicarbonate, thymol, tricalciun phosphate, zea mays (corn stach), zinc oxide, zinc stearate

  • Equate Medicated Body Powder Original

    labellabel

  • INGREDIENTS AND APPEARANCE
    MEDICATED BODY  POWDER
    menthol powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-724
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.42 g  in 283 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
    ACACIA (UNII: 5C5403N26O)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    MENTHYL SALICYLATE, (+/-)- (UNII: 43XOA705ZD)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    THYMOL (UNII: 3J50XA376E)  
    ZINC STEARATE (UNII: H92E6QA4FV)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    ZEA MAYS WHOLE (UNII: 1G5HNE09V8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-724-01283 g in 1 BOTTLE; Type 0: Not a Combination Product09/01/2020
    2NDC:79903-724-04113 g in 1 BOTTLE; 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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