Label: HYDROGEN PEROXIDE solution

  • NDC Code(s): 0869-0871-18, 0869-0871-43, 0869-0871-45, 0869-0871-72, view more
    0869-0871-82, 0869-0871-99
  • Packager: Vi-Jon, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 30, 2024

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

  • Active ingredient

    Hydrogen peroxide (stabilized) 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 one 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
    • sore mouth symptoms do not improve in 7 days
    • 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

    For First aid antiseptic:

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

    keep tightly closed and at controlled room temperature.  Do not shake bottle.  Hold away from face when opening.

  • Inactive ingredient

    purified water

  • Adverse reaction

    Distributed by: Vi-Jon, LLC.,

    8515 Page Ave.

    St. Louis, MO 63114

  • Principal Display Panel

    Swan

    Hydrogen Peroxide

    Topical Solution USP

    • First Aid Antiseptic/Oral Debriding Agent
    • For treatment of minor cuts & abrasions

    6 FL OZ (177 mL) 

    image description

  • INGREDIENTS AND APPEARANCE
    HYDROGEN PEROXIDE 
    hydrogen peroxide solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0869-0871
    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:0869-0871-72295 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/09/2017
    2NDC:0869-0871-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/09/2017
    3NDC:0869-0871-45946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/09/2017
    4NDC:0869-0871-18118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/09/201704/12/2021
    5NDC:0869-0871-99237 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/09/2017
    6NDC:0869-0871-82177 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/09/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/09/2017
    Labeler - Vi-Jon, LLC (088520668)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(0869-0871)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(0869-0871)