Label: ZEROQ FOOD- potassium carbonate liquid

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

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 September 28, 2020

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  • ACTIVE INGREDIENT

    potassium carbonate

  • INACTIVE INGREDIENT

    e-polylysine, dextrin, 1,2-propanediol, citric acid, tea catechin, hydroxypropylmethyl cellulose, water

  • PURPOSE

    Helps to kill bacteria and germs on foods, and remove harmful residues on meats and vegetables.

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

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

  • WARNINGS

    Use only according to instruction

    When using this product

    Avoid direct sunlight, keep in cool place.

    Keep out of reach of children

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    ZEROQ FOOD 
    potassium carbonate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80643-0004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE0.5 g  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80643-0004-1500 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 other09/21/2020
    Labeler - JISANG Co., Ltd. (694802124)
    Registrant - JISANG Co., Ltd. (694802124)
    Establishment
    NameAddressID/FEIBusiness Operations
    JISANG Co., Ltd.694802124manufacture(80643-0004)