Label: HYDROGEN PEROXIDE- 1169 hydrogen peroxide spray spray

  • NDC Code(s): 67777-015-07, 67777-015-08
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 16, 2024

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

View All Sections
  • Active Ingredient

    Hydrogen Peroxide 3%

  • Purpose

    First Aid Antiseptic

  • Use(s)

    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 • Over larege areas of the body • More than 1 week unless directed by a doctor

    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 • A rash or other allergic reaction develops

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    • Spray over affected area • May be covered with a sterile bandage • If bandaged, let dry first

    • Children under 12 years of age: Consult a doctor before use

  • Other Information

    Store at 20º-25ºC (68º-77ºF)

  • Inactive Ingredient

    Purified Water

  • Questions?

    1-888-Dynarex Monday - Friday, 9AM - 5PM EST.

  • Label

    1169_IN_MASTER1169 Label

  • INGREDIENTS AND APPEARANCE
    HYDROGEN PEROXIDE 
    1169 hydrogen peroxide spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-015
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE0.03 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeFREEFORMSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-015-0724 in 1 CASE02/29/2024
    1NDC:67777-015-0859.1 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/29/2024
    Labeler - Dynarex Corporation (008124539)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!