Label: HYDROGEN PEROXIDE spray

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated April 26, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Hydrogen Peroxide Topical Solution 3%

  • 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

    • in the eyes or apply over large areas of the body
    • longer than one week unless directed by a doctor

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    Stop use and ask a doctor if conditions persist or get worse.

    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 this product on the area 1 - 3 times daily
    • may be covered with a sterile bandage. If bandaged, let dry first.
  • Other Information

    • store at room temperature
  • Inactive ingredients

    purified water

  • Questions?

    1-866-651-3660

    Mon-Fri 8:00am-5:00pm EST

    Manufactured for American Safety & First Aid Osceola, IN 46561

    V1_11-7-19

  • Principal Display Panel – Bottle Label

    0661

    NDC 73598-0661-1

    Hydrogen
    Peroxide

    First Aid Antiseptic

    First Aid to Help
    Prevent Infection in
    Minor Cuts, Scrapes
    and Burns.

    American Safety
    & First Aid

    2 fl. oz. (59.1 ml)

    Principal Display Panel – Bottle Label
  • INGREDIENTS AND APPEARANCE
    HYDROGEN PEROXIDE 
    hydrogen peroxide spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73598-0661
    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:73598-0661-159.1 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/14/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM00402/14/2020
    Labeler - JHK Inc (867236309)
    Registrant - Safetec of America, Inc. (874965262)
    Establishment
    NameAddressID/FEIBusiness Operations
    Safetec of America, Inc.874965262MANUFACTURE(73598-0661)
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