Label: PUBE CHLORINE DIOXIDE DISINFECTION- pube chlorine dioxide disinfection tablets tablet

  • NDC Code(s): 81391-001-01, 81391-001-11
  • Packager: Guangdong Jiajie Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Updated January 4, 2024

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  • Active Ingredient(s)

    Sodium Chlorite 30.0%

  • Purpose

    Disinfection.

  • Use

    For external use only.

  • Warnings

    Keep away from direct sunlight.
    For external use only.

  • Do not use

    /

  • WHEN USING

    /

  • STOP USE

    /

  • KEEP OUT OF REACH OF CHILDREN

  • Directions

    Dissolve 1g of product into 1 Liter of purified water to generate 50mg -100mg of Chlorine Dioxide.

  • Other information

    Please follow the instructions in the user manual.

  • Inactive ingredients

    Sodium Carbonate, Anhydrous Sodium Sulfate,Citric Acid,Sodium Chloride,Boric Acid,Corn Starch.

  • Package Label - Principal Display Panel

    User Manual

    User Manual

    81391-001-01 Outer packaging

    81391-001-01 Outer packaging

    81391-001-11 inner packaging

    81391-001-11 inner packaging

  • INGREDIENTS AND APPEARANCE
    PUBE CHLORINE DIOXIDE DISINFECTION 
    pube chlorine dioxide disinfection tablets tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81391-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE30 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    BORIC ACID (UNII: R57ZHV85D4)  
    SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM CARBONATE (UNII: 45P3261C7T)  
    Product Characteristics
    ColorwhiteScorescore with uneven pieces
    ShapeROUNDSize12mm
    FlavorLIMEImprint Code No
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81391-001-0110 in 1 BAG03/30/2020
    1NDC:81391-001-111 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/30/2020
    Labeler - Guangdong Jiajie Technology Co., Ltd. (402971481)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Jiajie Technology Co., Ltd.402971481manufacture(81391-001)
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