Label: KO-C100- chlorine dioxide tablet, for solution

  • 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 November 23, 2022

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  • Active Ingredient(s)

    Chlorine Dioxide 0.1g/1g. Purpose: Sterilization, disinfection

  • Purpose

    Sterilization, disinfection

  • Use(s)

    It is suitable for environmental disinfection in public spaces, public transportation, schools, hospitals, stores, restaurants, homes, food factories, and animal husbandry.

  • Warnings

    External Use Only. Do not take orally.

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children.

  • Directions

    Take out 1 KO-100C Disinfectant, add it to a container filled with 1000c.c. water, let it stand for 1-3 minutes to dissolve into a light yellow disinfectant stock solution, and then distribute it to various containers for immediate use.

  • Other information

    • Store at a cool place
    • Valid period: 2 years
  • Inactive ingredients

    Citric Acid, Magnesium Sulfate, Sodium Bicarbonate, Sodium Chloride

  • Package Label - Principal Display Panel

    1g * 1000 tablet, NDC: 81797-701-13 Label

  • INGREDIENTS AND APPEARANCE
    KO-C100 
    chlorine dioxide tablet, for solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81797-701
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORINE DIOXIDE (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM) CHLORINE DIOXIDE0.1 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Product Characteristics
    ColoryellowScoreno score
    ShapeROUNDSize10mm
    FlavorEGG NOGImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81797-701-151000 in 1 PACKAGE04/09/2021
    1NDC:81797-701-001 g in 1 DOSE PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/09/2021
    Labeler - DONG FUH BIOTECH CO., LTD. (658813795)
    Establishment
    NameAddressID/FEIBusiness Operations
    DONG FUH BIOTECH CO., LTD.658813795manufacture(81797-701)