Label: NAOCLEAN E-WATER- sodium hypochlorite liquid

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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)