Label: QUALITY CHOICE HYDROGEN PEROXIDE WIPES- hydrogen peroxide cloth

  • NDC Code(s): 63868-184-40
  • Packager: Chain Drug Marketing Association, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 9, 2023

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

View All Sections
  • Drug Facts

  • Active ingredient

    Hydrogen peroxide (stabilized) 3%

    Purpose

    First aid antiseptic

  • Uses

    first aid to help prevent the risk of infection in:

    • minor cuts
    • scrapes 
    • burns
  • Warnings

    For external use only.

    Ask a doctor before use if you have

    • deep or puncture wounds 
    • animal bites 
    • serious burns

    When using this product

    • do not get in eyes
    • do not apply over large areas
    • do not use longer than 1 week unless directed by a doctor 

    Stop use and ask doctor

    if condition persists or gets 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
    • apply product on the affected area of the body 1 to 3 times a day
    • may be covered with a sterile bandage
    • if bandaged, let dry first
  • Other information

    • do not apply internally
    • keep canister tightly closed and at controlled room temperature 
    • hold away from face when opening
  • Inactive ingredient

    polysorbate 80, purified water

  • Package Labeling:

    label

  • INGREDIENTS AND APPEARANCE
    QUALITY CHOICE HYDROGEN PEROXIDE WIPES 
    hydrogen peroxide cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-184
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE0.03 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63868-184-4040 in 1 CANISTER09/01/2020
    14.5 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00309/01/2020
    Labeler - Chain Drug Marketing Association, Inc. (011920774)
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!