Label: BIOPURE 3 HYDROGEN PEROXIDE- hydrogen peroxide liquid

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

Drug Label Information

Updated December 9, 2024

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  • Drug Facts

  • Active ingredients

    Hydrogen Peroxide 3%

    Purpose

    First aid antiseptic

  • Uses

    • First aid to help prevent the risk of 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 punture wounds, animal bites or serious burns.

    Stop use and ask a doctor if

    • the condition persists or gets worse.
    • irritation, pain, or rendess 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.
    • spray a small amount of product on the affected area 1 to 3 times a day.
    • may be covered with sterile bandage. 
    • if bandaged, let dry first.
  • Other information

    • Store in a cool and well-ventillated place, keep tightly closed.
    • Protect from exposure to sunlight.
    • Protect from overheating/heating up.
    • Keep away from ignition source.
  • Inactive ingredients

    water

  • Questions?

    call 718-975-2586

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    BIOPURE 3 HYDROGEN PEROXIDE 
    hydrogen peroxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78691-021
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78691-021-50177 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/29/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/29/2023
    Labeler - Quest USA Corp (079869689)
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