Label: PURIGO- silicon oxide, potassium, borax, calcium carbonate liquid

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

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Drug Label Information

Updated September 6, 2017

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  • Active ingredient

    Silicon oxide, Potassium, Borax, Calcium carbonate

    Purpose

    Disinfectant Deodorant

  • Use

    Deodrant of multi-purpose (infant toys, baby bottle, pet, cook tools, bedding, musical instrument, the air in the room, clothes, closet, shoe rack, all sorts of odor removal and washing, and etc.)

  • WARNINGS

    1. Do not use for the purpose of drinking.
    2. Do not use in aluminum containers.
    3. Pay attention to high temperatures.
    4. Carefully release the lid before opening.
    5. Put in the shade.

    Keep out of reach of children

    Keep out of reach of children

  • Directions

    Spray more than 3 times a day, evenly.

  • INACTIVE INGREDIENT

    barley stone, zeolite, germanium, ferric chloride, sugar, additive, distilled water

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    PURIGO 
    silicon oxide, potassium, borax, calcium carbonate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71710-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM (UNII: RWP5GA015D) (POTASSIUM - UNII:RWP5GA015D) POTASSIUM9.3 g  in 100 mL
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE31 g  in 100 mL
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION18 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71710-0001-1500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/01/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/01/2017
    Labeler - Sun Jin Yu Ji Co (557829675)
    Registrant - Sun Jin Yu Ji Co (557829675)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sun Jin Yu Ji Co557829675manufacture(71710-0001) , label(71710-0001) , pack(71710-0001)
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