Label: CYANOX- chicory granule

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated March 13, 2018

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  • ACTIVE INGREDIENT

    chicory extract powder, aronia extract powder, kelp extract powder

  • INACTIVE INGREDIENT

    Natural raspberry flavor, enzyme treated stevia

  • PURPOSE

    • Application for a patent : Adjuvants and anticancer immuno-therapeutic agents comprising anthoyanin- fucoidan complex
    • Registration of a patent : Anthocyanin via Charge Complex with Anionic Polysaccharide Having Improved Stability, Composition Containing the Same, and Method for Preparing the Same

  • WARNINGS

    • Application for a patent : Adjuvants and anticancer immuno-therapeutic agents comprising anthoyanin- fucoidan complex
    • Registration of a patent : Anthocyanin via Charge Complex with Anionic Polysaccharide Having Improved Stability, Composition Containing the Same, and Method for Preparing the Same

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • INDICATIONS & USAGE

    Take 1 stick once a time, and twice a day

  • DOSAGE & ADMINISTRATION

    for oral use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CYANOX 
    chicory granule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72173-0001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHICORY LEAF (UNII: WBQ249COFR) (CHICORY LEAF - UNII:WBQ249COFR) CHICORY LEAF90 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ARONIA MELANOCARPA FRUIT (UNII: S935718Z2Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72173-0001-13 g in 1 POUCH; Type 0: Not a Combination Product03/14/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/14/2018
    Labeler - JBKLAB Co., Ltd (557838543)
    Registrant - JBKLAB Co., Ltd (557838543)
    Establishment
    NameAddressID/FEIBusiness Operations
    JBKLAB Co., Ltd.557838543manufacture(72173-0001) , label(72173-0001)
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Safety

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Related Resources

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