Label: KIMCHI LACTIC ACID 1000- lactobacillus plantarum granule

  • NDC Code(s): 70130-001-01, 70130-001-02
  • Packager: Biogenicskorea Co., LTD
  • 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 October 14, 2015

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  • ACTIVE INGREDIENT

    Lactobacillus plantarum 6.736%

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  • PURPOSE

    Immune Support

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  • INDICATIONS & USAGE

    Supporting immune System
    Helps healthy colon and intestinal flora

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  • DOSAGE & ADMINISTRATION

    Use once a day; for better result, use 3 packs daily

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  • WARNINGS

    Do not use if allergic to any ingredients

    When using this product, seek for health care professional if you are pregnant or nursing

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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of the children

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  • INACTIVE INGREDIENT

    Lactose powder, Glucose powder, Galactooligosaccharide, Fructooligosaccharide, Mandarin orange extract powder, Citron fruit juice powder, Orange flavor powder

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  • INGREDIENTS AND APPEARANCE
    KIMCHI LACTIC ACID 1000 
    lactobacillus plantarum granule
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:70130-001
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Lactobacillus Plantarum (UNII: QFC21096ON) (LACTOBACILLUS PLANTARUM - UNII:QFC21096ON) Lactobacillus Plantarum 0.101 g  in 1.5 g
    Inactive Ingredients
    Ingredient Name Strength
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
    TANGERINE (UNII: KH3E3096OO)  
    CITRUS JUNOS FRUIT (UNII: 53KHW58C1V)  
    ORANGE (UNII: 5EVU04N5QU)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:70130-001-02 30 in 1 CARTON
    1 NDC:70130-001-01 1.5 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 10/14/2015
    Labeler - Biogenicskorea Co., LTD (688466145)
    Registrant - Biogenicskorea Co., LTD (688466145)
    Establishment
    Name Address ID/FEI Business Operations
    Biogenicskorea Co., LTD 688466145 manufacture(70130-001)
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