Label: GREEN GUARD HYDROGEN PEROXIDE- hydrogen peroxide spray

  • NDC Code(s): 47682-334-02
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 16, 2024

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  • Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Hydrogen Peroxide 3.0%

  • PURPOSE

    Purpose

    First aid antiseptic

  • INDICATIONS & USAGE

    Uses

    First aid to help prevent infection in minor cuts, scrapes and burns

  • WARNINGS

    Warnings

    For external use only.

  • DO NOT USE

    Do not use

    • near eyes or mucous membranes
    • on deep or puncture wounds, animal bites, or serious burns consult a doctor
    • on large areas of the body
  • STOP USE

    Stop use and ask a doctor if the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    Directions

    • spray over affected area
    • if bandaged, let dry first
    • not to be used on children under 12 years of age
  • INACTIVE INGREDIENT

    Inactive ingredient

    purified water

  • QUESTIONS

    Questions or comments? 1-800-869-6970

  • Green Guard Hydrogen Peroxide Spray Label

    Hydrogen Peroxide Spray

    Hydrogen Peroxide 3%

    First Aid Antiseptic

    Treats minor cuts, scrapes and abrasions

    Helps prevent infection

    Store at 68°-77°F (20°-25°C)

    Green Guard®

    2 fl oz (59.1 mL)

    GG Hydrogen

  • INGREDIENTS AND APPEARANCE
    GREEN GUARD HYDROGEN PEROXIDE 
    hydrogen peroxide spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-334
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE30 mL  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-334-020.0591 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/01/2021
    Labeler - Unifirst First Aid Corporation (832947092)
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