Label: CHLORINE DIOXIDE AIR DISINFECTANT powder

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

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Drug Label Information

Updated May 6, 2020

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  • DOSAGE & ADMINISTRATION

    store in dark, cool, dry,ventilated_ place, do not contact with acid, organic matter, inflammables and other strong reducing agent or storage together

  • INACTIVE INGREDIENT

    Anhydrous sodium sulfate

    Calciun chloride

    Sodium bisulfate

    Sodium chlorite

  • INDICATIONS & USAGE

    Open the box and aluminum foil bag,according to the configuration of 1m/unit enclosed space, the operation time is 1h

  • ACTIVE INGREDIENT

    Chlorine Dioxide

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PURPOSE

    Disinfection
    Sterilization

  • WARNINGS

    1. External disinfectant should not be taken orally;Keep out of reach of children;
    2. Should not be mixed with other disinfectants, alkali or organic matter;
    3. This product can bleach,It shall not be used for disinfection of metal articles;
    4. Avoid contact with skin and inhalation of high concentration disinfectant;
    5. The product should be kept away from fire and heat source;
    6. Do not use in wet places such as rain, high temperature and places with long time sun exposure;
    7. Do not breathe near the nose or directly;
    8. If the. disinfectant accidentally touches. the eyes,rinse with water immediately, or seek medical advice in severe cases.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CHLORINE DIOXIDE AIR DISINFECTANT 
    chlorine dioxide air disinfectant powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55090-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORINE DIOXIDE (UNII: 8061YMS4RM) (CHLORINE DIOXIDE - UNII:8061YMS4RM) CHLORINE DIOXIDE130 mg  in 6.5 g
    Inactive Ingredients
    Ingredient NameStrength
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
    SODIUM BISULFATE (UNII: BU8V88OWIQ)  
    SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750)  
    SODIUM CHLORITE (UNII: G538EBV4VF)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55090-001-016.5 g in 1 BOTTLE; Type 0: Not a Combination Product05/06/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/06/2020
    Labeler - Chengdu Xinyi Kaiwei Medical Equipment Co., Ltd. (550900665)
    Establishment
    NameAddressID/FEIBusiness Operations
    Chengdu Xinyi Kaiwei Medical Equipment Co., Ltd.550900665manufacture(55090-001)
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