Label: ARONOX- chicory powder

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

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 September 24, 2018

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  • ACTIVE INGREDIENT

    chicory extract

  • INACTIVE INGREDIENT

    aronia extract powder, enzyme treated stevia

  • PURPOSE

    in the fruit of Aronia, a large amount of red anthraanthocyanin is contained, which is very powerful antioxidant. It acts as a powerful cell signaling molecule (CSM), immunity enhancing action, blood flow improving action, and stem cell activating action were excellent.

  • WARNINGS

    1. Open the pouch slowly so that the contents may come off when opening.
    2. The edge of the pouch is sharp, so be careful not to let your skin dry when you are eating or carrying it.
    3. Do not heat the microwave oven as it is pouch packaging.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • INDICATIONS & USAGE

    Take 1 pouch once or twice a day

  • DOSAGE & ADMINISTRATION

    for oral use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    ARONOX 
    chicory powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72173-0003
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHICORY LEAF (UNII: WBQ249COFR) (CHICORY LEAF - UNII:WBQ249COFR) CHICORY LEAF70.45 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ARONIA MELANOCARPA FRUIT (UNII: S935718Z2Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72173-0003-12 g in 1 POUCH; Type 0: Not a Combination Product09/25/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/25/2018
    Labeler - JBKLAB Co., Ltd (557838543)
    Registrant - JBKLAB Co., Ltd (557838543)
    Establishment
    NameAddressID/FEIBusiness Operations
    JBKLAB Co., Ltd.557838543manufacture(72173-0003) , label(72173-0003)