Label: YOBISIN- rehmannia root, angelica gigas root tablet

  • 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 December 16, 2023

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  • ACTIVE INGREDIENT

    rehmannia root, angelica gigas root, akebia stem, scutellaria root, alisma rhizome, plantago seed, licorice, gardenia fruit, gentian root and rhizome, cinnamomum cassia presl, raw ginger, rhubarb, ephdra heab, forsythia fruit

  • INACTIVE INGREDIENT

    magnesium stearate, corn starch, polyethylene glycol 6000, hypromellose 2910

  • PURPOSE

    bladder qatar, urethritis, kidney disease, nephrotic syndrome, edema

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    adults: 3~6 tablets twice a day

    7 to 14 years old: 2-3 tablets twice a day

  • WARNINGS

    do not take this medicine if you have following symptoms

    children under 6 years old

    women who are likely to be pregnant or pregnant

    breastfeeding

  • DOSAGE & ADMINISTRATION

    for oral use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    YOBISIN 
    rehmannia root, angelica gigas root tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72988-0012
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    RHUBARB (UNII: G280W4MW6E) (RHUBARB - UNII:G280W4MW6E) RHUBARB16.7 mg
    REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ) (REHMANNIA GLUTINOSA ROOT - UNII:1BEM3U6LQQ) REHMANNIA GLUTINOSA ROOT416.7 mg
    ANGELICA GIGAS ROOT (UNII: 32766B2FHX) (ANGELICA GIGAS ROOT - UNII:32766B2FHX) ANGELICA GIGAS ROOT416.7 mg
    AKEBIA STEM (UNII: 531B9G152H) (AKEBIA STEM - UNII:531B9G152H) AKEBIA STEM416.7 mg
    SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) (SCUTELLARIA BAICALENSIS ROOT - UNII:7J95K7ID2S) SCUTELLARIA BAICALENSIS ROOT250 mg
    LICORICE (UNII: 61ZBX54883) (LICORICE - UNII:61ZBX54883) LICORICE125 mg
    ALISMA PLANTAGO-AQUATICA ROOT (UNII: 6DXR2088WL) (ALISMA PLANTAGO-AQUATICA ROOT - UNII:6DXR2088WL) ALISMA PLANTAGO-AQUATICA ROOT250 mg
    FORSYTHIA SUSPENSA FRUIT (UNII: P4793M1ES5) (FORSYTHIA SUSPENSA FRUIT - UNII:P4793M1ES5) FORSYTHIA SUSPENSA FRUIT16.7 mg
    PLANTAGO SEED (UNII: 9C60Y73166) (PLANTAGO SEED - UNII:9C60Y73166) PLANTAGO SEED250 mg
    GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER16.7 mg
    CHINESE CINNAMON (UNII: WS4CQ062KM) (CHINESE CINNAMON - UNII:WS4CQ062KM) CHINESE CINNAMON16.7 mg
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    ColorbrownScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code T;2
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72988-0012-120 in 1 PACKAGE; Type 0: Not a Combination Product04/24/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/22/2019
    Labeler - Lydia Co., Ltd. (695735569)
    Registrant - Lydia Co., Ltd. (695735569)
    Establishment
    NameAddressID/FEIBusiness Operations
    I World Pharmaceutical Co., Ltd.688222857manufacture(72988-0012)
    Establishment
    NameAddressID/FEIBusiness Operations
    Lydia Co., Ltd.695735569label(72988-0012)