Label: ALL CLEAN WATER- hypochlorous acid liquid

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

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Drug Label Information

Updated December 16, 2021

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  • inactive ingredient

    Water

  • Active Ingredients

    Hypochlorous Acid

  • Direction

    Spray on hands or spray where disinfection is needed

  • Do not use

    For external use only. Discontinue if irritation or rash occurs.

    Do not use on broken or abraded skin.

  • Use

    Hand sanitizer to help reduce bacteria that potentially can cause disease.
    For use when soap and water are not avaliable.

  • Warnings

    Do not spray on clothes because it can stain.

    Do not use on broken or abraded skin.

  • Keep out of reach of children

    Keep out of reach of children.

  • Stop use and ask a doctor.

    Take care not to get into the eye.

    If swallowed contact your doctor immediately

  • Stop use and ask a doctor.

    if the following symptoms appear,Stop use and immediately consult a doctor: rash, erythema, itching, edema or any other skin irritation.

  • Other information

    Keep out of direct sunlight.

    Take care not to get into the eye. Store below 75.2℉

  • indication

    After use, properly close the product to avoid drying out or spilling.

    Take an appropriate amount on your hands and rub thoroughly to dry.

  • purpose

    antimicrobial

  • LABEL

    79186-301-01

    60ML

    79186-301-03

    79186-301-02 150

    500ML

  • INGREDIENTS AND APPEARANCE
    ALL CLEAN WATER 
    hypochlorous acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79186-301
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.07 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 99.93 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79186-301-0160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/25/2020
    2NDC:79186-301-02500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/25/2020
    3NDC:79186-301-03150 mL in 1 BOTTLE; Type 0: Not a Combination Product09/06/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/25/2020
    Labeler - MISSIWOMAN COSMETIC (695520588)
    Registrant - MISSIWOMAN COSMETIC (695520588)
    Establishment
    NameAddressID/FEIBusiness Operations
    MISSIWOMAN COSMETIC695520588manufacture(79186-301)
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