Label: CLEAN-US PURICHLO SANITIZER-SPRAY- hypochlorous acid liquid

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

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Drug Label Information

Updated September 22, 2020

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  • Active ingredients

    Hypochlorous Acid 0.005%

  • Purpose

    Sanitizer

  • Uses

    Purpose of sterilizing the surface of instruments and objects.

  • Warning

    This Products are for use on surface, Not humans.

    Follow the contact time as directed in the directions.

    Do not touch the surface during the contact time.

    Do not dilute, use the solution as is.

  • Stop use and ask a doctor if irritation or redness occurs.

    Do not inhale or ingest.

  • Keep out of reach of children.

    Make sure to supervise the use of products by children, the elderly, the disabled, and others who vulnerable to the use of products.

  • Directions

    Spray on the surface of sterilizing object in a wide range.

    Spray on a target that requires sterilization and let it dry naturally or wipe with a dry towel after 30 seconds.

    If you can’t spray directly on the surface, you can spray to the clean cloth and wipe it off.

  • Other information

    If this product is exposed to external air for a long time it may react with UV or air and be restored to water.

    Keep it sealed and store in a cool and dark place.

  • Inactive ingredients

    Water 99.995%

  • Package Label

    79543-201-01 60ml Label

    79543-201-02 500ml Label

  • INGREDIENTS AND APPEARANCE
    CLEAN-US PURICHLO SANITIZER-SPRAY 
    hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79543-201
    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:79543-201-0160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/10/2020
    2NDC:79543-201-02500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/21/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/10/2020
    Labeler - KUMWON INTERNATIONAL INC. (694803493)
    Registrant - Multibio Co., Ltd (693713128)
    Establishment
    NameAddressID/FEIBusiness Operations
    Multibio Co., Ltd693713128manufacture(79543-201)
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