Label: MEDPRIDE MEDICATED BODY POWDER POWDER- menthol, zinc oxide 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 July 31, 2023

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  • Drug Facts Active Ingredients

    Menthol 0.15 %

    Zinc Oxide 1.0%

  • Purpose

    Anti-itch

    Skin Protectant

  • 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.

  • Keep out of reach of children

    Keep out of reach of children. In case of accidential ingestion, get medical help or contact a Poison Control Center right away.

  • Warnings

    For external use only

  • When usin this product

    • Avoid contact with eyes.
    • Keep away from face and mouth to avoid inhalation
    • Not for genital area.
  • Stop use and ask a doctor if

    • condition worsens
    • symptoms do not get better within 7 days or clear up and occur again within a few days
  • Directions

    • adults and children 2 years and older, apply freely up to 3 or 4 times daily
    • under 2 years: ask a doctor before using
    • for best results, dry skin thoroughly before use
  • Inactive Ingredients

    Corn Starch, Eucalyptol, Gum Talha, Methyl Salicylate, Salicylic Acid, Sodium Bicarbonate, Thymol, Tricalcium Phosphate, Zinc Stearate

  • PRINCIPAL DISPLAY PANEL

    Principal Display and Drug Fact Panel

  • INGREDIENTS AND APPEARANCE
    MEDPRIDE MEDICATED BODY POWDER  POWDER
    menthol, zinc oxide powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52410-4031
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.15 g  in 100 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    GUM TALHA (UNII: H18F76G097)  
    EUCALYPTOL (UNII: RV6J6604TK)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    THYMOL (UNII: 3J50XA376E)  
    ZINC STEARATE (UNII: H92E6QA4FV)  
    TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52410-4031-0283 g in 1 BOTTLE; Type 0: Not a Combination Product10/05/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34810/05/2021
    Labeler - Shield Line LLC (078518916)
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