Label: NAOCLEAN E-WATER- sodium hypochlorite liquid

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

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Drug Label Information

Updated August 7, 2020

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  • ACTIVE INGREDIENT

    Sodium hypochlorite

  • PURPOSE

    For disinfecting to remove bacteria

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF THE CHILDREN

  • INDICATIONS & USAGE

    ● Shake thoroughly before use.

    ● Without mixing any other ingredients or diluting with water, spray towards the intended area and/or objects.

    ● Store in a cool place away from direct sunlight

  • WARNINGS

    ● Do not drink as it is not intended for drinking.

    ● Do not immerse or spray for kitchen knives, aluminum containers, etc. as corrosion may occur.

    ● Be careful of discoloration of colored clothes.

    ● Do not leave for a long time in heat or ultraviolet rays as lower sterilization.

    ● Do not use for any other purpose. (For external use only.)

    ● Avoid contact with eyes. If contact occurs, flush with water.

    ● Stop use and ask doctor if, in rare instances, redness and irritation develop and persists for more than 72 hours.

    ● Keep out of reach of children. If swallowed, contact a physician.

  • DOSAGE & ADMINISTRATION

    for external use only

  • INACTIVE INGREDIENT

    water

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    NAOCLEAN E-WATER 
    sodium hypochlorite liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76876-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) (HYPOCHLORITE ION - UNII:T5UM7HB19N) SODIUM HYPOCHLORITE0.02 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76876-0002-120000 mL in 1 CONTAINER; Type 0: Not a Combination Product08/08/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/08/2020
    Labeler - D&D Electronics Co Ltd (557825263)
    Registrant - D&D Electronics Co Ltd (557825263)
    Establishment
    NameAddressID/FEIBusiness Operations
    D&D Electronics Co Ltd695625894manufacture(76876-0002)
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