Label: MEDIBLUE- hypochlorous acid liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated February 18, 2022

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  • ACTIVE INGREDIENT

    Hypochlorous acid 0.005%

  • PURPOSE

    Antiseptic

  • USES

    Multi purpose sterilization, disinfection

  • WARNINGS

    For external use only

  • WHEN USING THIS PRODUCT

    Keep out of eyes, in case of contact with eyes, flush thoroughly with water

    Avoid contact with broken skin

    Do not inhale or ingest

  • WHEN USING THIS PRODUCT

    Stop immediately and consult a doctor it you experience skin imitation or rash develops

  • WHEN USING THIS PRODUCT

    Keep out of reach of children. if swallowed, get medical help or contact a posion control center right away.

  • DIRECTIONS

    Spray the sterilizing object in a wide range

    Please supervise when using the product by children, the elderly, the disabled, etc.

  • OTHER INFORMATION

    Read the directions and warnings before use

    If exposed to the air, sterilization may be reduced due to water-soluble, so keep the container sealed.

    Avoid freezing and excessive heat above 40 degree C (104 degree F) 40C(104F)

  • INACTIVE INGREDIENTS

    Water

  • PACKAGE LABEL

    500ml NDC: 76847-302-01 Label

    4000ml NDC: 76847-302-02 Label

    20000ml NDC: 76847-302-03 Label

  • INGREDIENTS AND APPEARANCE
    MEDIBLUE 
    hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76847-302
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.005 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 99.995 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76847-302-01500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/30/2020
    2NDC:76847-302-024000 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/2020
    3NDC:76847-302-0320000 mL in 1 BOTTLE; Type 0: Not a Combination Product07/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/30/2020
    Labeler - Multibio Co., Ltd (693713128)
    Registrant - Multibio Co., Ltd (693713128)
    Establishment
    NameAddressID/FEIBusiness Operations
    Multibio Co., Ltd693713128manufacture(76847-302)
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