Label: HYDROGEN PEROXIDE liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 5, 2023

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

View All Sections
  • Active Ingredient

    Hydrogen Peroxide (stabilized) 3 %

    Purpose

    First Aid Antiseptic Oral debriding agent

  • Inactive Ingredients:

    Purified water

  • Uses:

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

    Aids in the removal of phlegm, mucus, or other secretions associated with ocassional sore mouth.

  • Warnings:

    For extenal use only.

    Do not use:

    • In the eyes or apply over large areas of the body.
    • Longer than 1 week.

    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.

    Ask a doctor before use if 

    you have deep or puncture wounds, animal bites or serious burns.

    Keep out of reach of Children 

    if swallowed, get medical help or contact a poison control center right away.

  • Directions

    First aid antiseptic

    Oral debriding agent:

    • Clean the affected area.
    • Apply 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.
    • Mix with an equal amount of water.
    • swish around in the mouth over the affected area for at least 1 minute, and then spit out.
    • Use up to 4 times daily after meals and at bedtime.
    • Children under 12 years of age should be supervised in the use.
    • Children under 2 years of age: consult a dentist, doctor.
  • Other Information

    • Keep tightly closed and at controlled room temperature.
    • Do not shake bottle.
    • Hold away form face when opening.
  • Question or comments?

    Call 956 728-8899

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    HYDROGEN PEROXIDE 
    hydrogen peroxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67326-353
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67326-353-01473 mL in 1 BOTTLE; Type 0: Not a Combination Product10/25/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02210/25/2017
    Labeler - Degasa, S.A. de C.V. (812771980)
    Registrant - Degasa, S.A. de C.V. (812771980)
    Establishment
    NameAddressID/FEIBusiness Operations
    Degasa, S.A. de C.V.812771980manufacture(67326-353)
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!