Label: APLICARE- hydrogen peroxide solution

  • NDC Code(s): 52380-1013-3, 52380-1013-4
  • Packager: Aplicare Products LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 18, 2025

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  • Active Ingredient

    Hydrogen peroxide USP 3% w/v

  • Purpose

    First aid antiseptic

  • Use

    • first aid to help decrease the risk of skin infection in minor cuts, scrapes, and burns
  • Warnings

    For external use only

    Do not use

    • in the eyes or apply over large areas of the body
    • longer than 1 week

    Ask a doctor before use if you have

    deep or puncture wounds, animal bites, or serious burns

    Stop use and ask a doctor if

    • the condition persists or gets worse
    • irritation, pain, or redness persists or worsens
    • swelling, rash, or fever develops

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • clean the affected area
    • apply a small amount of this product on the area 1 to 3 times daily
    • may be covered with a sterile bandage
    • if bandaged, let dry first
  • Other information

    • not made with natural rubber latex
    • protect from freezing, avoid excessive heat
  • Inactive ingredient

    water

  • Manufacturing Information

    www.medline.com ©2024 Medline Industries, LP
    Aplicare is a registered trademark of Medline Industries, LP.
    Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093 USA

    1-800- MEDLINE.

    Made in China. V1 RK24JJS

  • Package Label

    pouch label

  • INGREDIENTS AND APPEARANCE
    APLICARE 
    hydrogen peroxide solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52380-1013
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE3 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52380-1013-330 mL in 1 PACKET; Type 0: Not a Combination Product02/01/2025
    2NDC:52380-1013-420 in 1 BOX02/01/2025
    2NDC:52380-1013-330 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/01/2025
    Labeler - Aplicare Products LLC (081054904)
    Registrant - Medline Industries, LP (025460908)
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