Label: SSANGBI TANG- galgeun-tang extract liquid

  • NDC Code(s): 73442-0008-1
  • Packager: I World Pharmaceutical Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated November 9, 2019

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  • ACTIVE INGREDIENT

    galgeun-tang extract (pueraria lobata ohwi, perilla leaf, raw ginger, jujube, peony root, licorice, cinnamon bark)

  • PURPOSE

    cold, flu, other minor aches and pains due to headache and muscular aches

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    take 1 pouch 3 times a day

  • WARNINGS

    do not intake if the product is found to have expired or corrupted

    when using this product be aware that the contents may flow when opening

    stop use and ask a doctor if you have certain body types and allergies, it can cause a severe allergic reaction

  • INACTIVE INGREDIENT

    water, liquid fructose

  • DOSAGE & ADMINISTRATION

    For oral use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    SSANGBI TANG 
    galgeun-tang extract liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73442-0008
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ) GINGER1.121 g  in 100 mL
    PERILLA FRUTESCENS LEAF (UNII: T4L5881Y68) (PERILLA FRUTESCENS LEAF - UNII:T4L5881Y68) PERILLA FRUTESCENS LEAF1.121 g  in 100 mL
    PUERARIA MONTANA VAR. LOBATA WHOLE (UNII: D295OFK7E1) (PUERARIA MONTANA VAR. LOBATA WHOLE - UNII:D295OFK7E1) PUERARIA MONTANA VAR. LOBATA WHOLE2.242 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    FRUCTOSE (UNII: 6YSS42VSEV)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73442-0008-180 mL in 1 POUCH; Type 0: Not a Combination Product10/08/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/08/2019
    Labeler - I World Pharmaceutical Co., Ltd. (688222857)
    Registrant - I World Pharmaceutical Co., Ltd. (688222857)
    Establishment
    NameAddressID/FEIBusiness Operations
    I World Pharmaceutical Co., Ltd688222857manufacture(73442-0008)
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