Label: GREEN GUARD FIRST AID ANTISEPTIC- hydrogen peroxide spray

  • NDC Code(s): 78495-152-01
  • Packager: Ultra Distributors Inc
  • 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 December 21, 2020

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  • Active ingredient

    Hydrogen Peroxide 3.0%

  • Purpose

    First aid antiseptic

  • Uses

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

  • Warnings

    For external use only.

  • 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 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.

  • Directions

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

  • Inactive ingredient

    purified water

  • Questions or comments?

    1-800-869-6970

  • SPL UNCLASSIFIED SECTION

    Treats minor cuts, scrapes and abrasions

    Helps prevent infection

    Store at 68°-77°F(20°-25°℃)

  • PRINCIPAL DISPLAY PANEL

    image of bottle label

  • INGREDIENTS AND APPEARANCE
    GREEN GUARD FIRST AID ANTISEPTIC 
    hydrogen peroxide spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78495-152
    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:78495-152-010.0591 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/19/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/19/2020
    Labeler - Ultra Distributors Inc (007160073)
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