Label: HYDROGEN PEROXIDE liquid

  • NDC Code(s): 47682-304-02, 47682-304-06
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 16, 2024

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    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

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

    Stop use and ask a doctor if

    • redness, irritation, swelling or pain persists or increases
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    • spray over affected area
    • if bandaged, let dry first
  • OTHER SAFETY INFORMATION

    Other information

    • store at room temperature
  • 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 room temperature

    GREEN GUARD®

    2 fl oz (59.1 mL)

    3004

  • INGREDIENTS AND APPEARANCE
    HYDROGEN PEROXIDE 
    hydrogen peroxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-304
    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:47682-304-060.118 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/10/201304/02/2018
    2NDC:47682-304-020.0591 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/10/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00312/10/2013
    Labeler - Unifirst First Aid Corporation (832947092)