Label: VIRUS BARRIER PLUS- sodium chlorite stick

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

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Drug Label Information

Updated July 30, 2020

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  • Active Ingredient

    SODIUM CHLORITE 20%

  • Purpose

    Viral Removal, Removal of Mold, Sterilization, Removal of Allergic substances, Deodorization, Prevention of Rhinitis

  • Usage of Case

    - It is available for using the employee card, cerdit card or name card.

    - After removing the strap, it can use the clip.

    - It can put in the breast pocket.

    - When sleeping, it is better to put near by the bed.

    - It is good to put in the car or the refrigerator.

  • Caution

    Do not eat or do not put in the mouth.

    When the product is put in the eye, wash down with the water.

  • Caution

    When using Virus Barrier Plus, please ask a doctor if you feel strange.

  • Caution

    Keep out of reach of children.

  • Directions

    1 Open the Chlorine Dioxide from the sealed package.

    2 Put the Chlorine Dioxide in the case.

    3 Close the case.

    4 Connect the necklace strap on the top of case.

    5 The case can be used by the employee card or card holder.

  • Inactive Ingredient

    SEPIOLITE, SODIUM HYDROXIDE

  • Package Label

    5g NDC: 79928-201-01 Label 1

    5g NDC: 79928-201-01 Label 2

  • INGREDIENTS AND APPEARANCE
    VIRUS BARRIER PLUS 
    sodium chlorite stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79928-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE20 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    MAGNESIUM TRISILICATE (UNII: C2E1CI501T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79928-201-015 g in 1 CASE; Type 0: Not a Combination Product07/31/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/31/2020
    Labeler - Wooju Mulsan Co., Ltd (690161846)
    Registrant - Wooju Mulsan Co., Ltd (690161846)
    Establishment
    NameAddressID/FEIBusiness Operations
    Wooju Mulsan Co., Ltd690161846manufacture(79928-201)
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