Label: CLEANING-S- potassium carbonate 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 January 1, 2018

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  • ACTIVE INGREDIENT

    Potassium carbonate

  • INACTIVE INGREDIENT

    Polysorbate20, Polysorbate80, Coconut oil, etc

  • PURPOSE

    Antibacterial

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children
     Do not swallow. In case of accidental ingestion, seek professional assistance.

  • INDICATIONS & USAGE

    Hygienic disinfectant especially suited for cleaning carpets, furniture, bedding, kitchens, bathrooms, and all types of kitchen utensils. Cleans floors, walls and counter tops. Safe for children and infant baby toys and bottles.

  • WARNINGS

    Warnings
    For external use only
    Do not use when liquid comes in contact with eyes, rinse immediately with water and consult the doctor.
    When using this product

    • Do not apply on other parts of the body
    • Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

    Store at room temperature

  • DOSAGE & ADMINISTRATION

    Directions
    For hygienic disinfection, this product can be used directly to the surface. Also, you can dilute one part product with two parts water.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CLEANING-S 
    potassium carbonate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71957-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71957-0001-1500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/02/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/02/2018
    Labeler - NARO, INC. (694590211)
    Registrant - NARO, INC. (694590211)
    Establishment
    NameAddressID/FEIBusiness Operations
    NARO, INC.694590211manufacture(71957-0001)