Label: CLOON STICK- sodium chlorite, citric cid 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 February 21, 2022

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  • ACTIVE INGREDIENT

    sodium chlorite, citric acid

  • INACTIVE INGREDIENT

    water

  • PURPOSE

    for objects to sterilize virus, bacteria and fungi etc

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF THE CHILDREN

  • INDICATIONS & USAGE

    This product can not be eaten. And do not use it for other purposes

    Avoid using in places exposed to high temperatures and direct sunlight for prolonged periods of time.

    patched or put on place needed sterilization and deodorization.

  • WARNINGS

    If you feel irritation in an enclosed space, provide enough ventilation

    If the product comes into contact with the skin for a long time, itching may be caused.
    Wash it thoroughly with running water and immediately consult a doctor if there is any abnormality.

  • DOSAGE & ADMINISTRATION

    for keeping freshness through sterilizing and disinfecting microbial(fungi, bacteria)

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CLOON STICK 
    sodium chlorite, citric cid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77130-0005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID5 g  in 100 g
    SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77130-0005-310 g in 1 PACKAGE; Type 0: Not a Combination Product01/15/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/15/2022
    Labeler - Sejin E&P Co., Ltd. (694459360)
    Registrant - Sejin E&P Co., Ltd. (694459360)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sejin E&P Co., Ltd.694459360manufacture(77130-0005)