Label: CHIDANGWON 300  - lagerstroemia indica whole tablet 

  • NDC Code(s): 53144-4001-1
  • Packager: Yein Trading & Global Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 01/13

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  • ACTIVE INGREDIENT

    banaba alcohol extract powder
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  • INACTIVE INGREDIENT

    Mixed plant extract powder 80.125% (Lactose 75%, Pueraria lobata Ohwi Root 5%, Glycyrrhiza uralensis 4%, Cinnamon 4%, Anmwon 4%, Cornus officinalis 4%, Leaves of Morus alba Linne 4%), Chaga mushroom extract powder (mycelium culture) 5%, Cultured Wild ginseng root powder 5%, Hydroxypropylmethyl-cellulose 4%, Carboxymethylcellulose calcium 2%, Magnesium stearate 1%, Gardenia Yellow 0.375%

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  • PURPOSE

    - treatment of diabetes
    - lowering blood sugar
    - prevention and treatment of diabetic complications
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  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children
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  • INGREDIENTS AND APPEARANCE
    CHIDANGWON 300  
    lagerstroemia indica whole tablet
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:53144-4001
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LAGERSTROEMIA INDICA WHOLE (LAGERSTROEMIA INDICA WHOLE) LAGERSTROEMIA INDICA WHOLE 0.018 
    Inactive Ingredients
    Ingredient Name Strength
    LACTOSE  
    PUERARIA MONTANA VAR. LOBATA ROOT  
    GLYCYRRHIZA URALENSIS  
    CINNAMON  
    CORNUS OFFICINALIS FRUIT  
    MORUS ALBA WHOLE  
    HYPROMELLOSES  
    CARBOXYMETHYLCELLULOSE CALCIUM  
    MAGNESIUM STEARATE  
    Product Characteristics
    Color brown (light brown) Score no score
    Shape OVAL (pill) Size 15mm
    Flavor Imprint Code 3;hp;x
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:53144-4001-1 120 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 01/05/2013
    Labeler - Yein Trading & Global Co., Ltd (557803795)
    Registrant - Yein Trading & Global Co., Ltd (557803795)
    Establishment
    Name Address ID/FEI Business Operations
    Han Kook Sin Yak Pharmaceutical Co., Ltd. 689277536 manufacture(53144-4001)
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