HYDROGEN PEROXIDE LIQUID [MEDICAL CHEMICAL CORPORATION]

HYDROGEN PEROXIDE LIQUID [MEDICAL CHEMICAL CORPORATION]
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NDC 12745-202-01, 12745-202-02, 12745-202-03
Set ID f6d677b8-fa89-4efb-984a-fd98e3e590e8
Category HUMAN OTC DRUG LABEL
Packager Medical Chemical Corporation
Generic Name
Product Class
Product Number
Application Number PART333A
  • PURPOSE

    Usage: Intended for use as a general purpose topical antiseptic for first-aid treatment of minor cuts and abrasions.  In case of deep or puncture wounds consult a physician.  Discontinue use and get medical attention if redness, irritation or infection develops.

  • ACTIVE INGREDIENT

    Active ingredient: hydrogen peroxide, 3% w/v in water.

  • KEEP OUT OF REACH OF CHILDREN

    For External Use Only.  Do not use in eyes or over large areas of the body.  Keep out of the reach of children.

  • INDICATIONS & USAGE

    Usage: Intended for use as a general purpose topical antiseptic for first-aid treatment of minor cuts and abrasions.  In case of deep or puncture wounds consult a physician.  Discontinue use and get medical attention if redness, irritation or infection develops.

  • WARNINGS

    For External Use Only.  Do not use in eyes or over large areas of the body.  Keep out of the reach of children.

  • DOSAGE & ADMINISTRATION

    For oral hygiene, dilute with an equal volume of water and gargle for about one minute.  Rinse with water.  In case of accidental ingestion contact a physician or a poison control center.

  • INACTIVE INGREDIENT

    Active ingredient: hydrogen peroxide, 3% w/v in water.

  • PRINCIPAL DISPLAY PANEL

    h2o2label.jpg

    Hydrogen Peroxide Label

  • INGREDIENTS AND APPEARANCE
    HYDROGEN PEROXIDE 
    hydrogen peroxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12745-202
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE8.57 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:12745-202-0159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/21/1980
    2NDC:12745-202-02118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/21/1980
    3NDC:12745-202-033785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/21/1980
    4NDC:12745-202-04208175 mL in 1 DRUM; Type 0: Not a Combination Product07/21/1980
    5NDC:12745-202-05946250 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product07/21/1980
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/21/1980
    Labeler - Medical Chemical Corporation (008496861)
    Establishment
    NameAddressID/FEIBusiness Operations
    Medical Chemical Corporation008496861manufacture(12745-202)

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