Label: AV-1000- sodium chlorite, citric cid powder

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated February 17, 2022

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  • ACTIVE INGREDIENT

    sodium chlorite 0.05%

    citric acid 0.06%

  • INACTIVE INGREDIENT

    magnesium silicate, aluminum silicate, rheology modifier

  • PURPOSE

    for objects to sterilize virus, vacteria 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.

    Put or Inserted in employee ID case, handbag, wallet, pocket or mask storage case.

  • WARNINGS

    For objects use only

    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 objects use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    AV-1000 
    sodium chlorite, citric cid powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77130-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID0.06 g  in 100 g
    SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6) SODIUM CHLORITE0.05 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM SILICATE (UNII: 9B9691B2N9)  
    ALUMINUM SILICATE (UNII: T1FAD4SS2M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77130-0001-18 g in 1 PACKAGE; Type 0: Not a Combination Product05/02/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/02/2020
    Labeler - Sejin E&P Co., Ltd. (694459360)
    Registrant - Sejin E&P Co., Ltd. (694459360)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sejin E&P Co., Ltd.694459360manufacture(77130-0001)
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