Label: JEGAMSAN EXTRACT- lonicera flower, acetaminophen, dextromethorphan hydromide granule

  • NDC Code(s): 73442-0013-1
  • Packager: I World Pharmaceutical 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 September 16, 2020

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  • ACTIVE INGREDIENT

    Lonicera Flower(KP)
    Acetaminophen
    Dextromethorphan Hydrobromide

  • PURPOSE

    throat pain due to cold, thirst, cough, headache

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    for adults take 1 pouch per intake, 3 times a day, before or between meals

  • WARNINGS

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • INACTIVE INGREDIENT

    Forsythia Fruit(KP), Mentha Herb(KP), Platycodon Root(KP), Lophatheri Herba(KHP), Schizonepeta Spike(KP), Glycine Semen, Arctium Fruit(KP), Gazelle Horn(KHP)

  • DOSAGE & ADMINISTRATION

    For oral use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    JEGAMSAN EXTRACT 
    lonicera flower, acetaminophen, dextromethorphan hydromide granule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73442-0013
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U) (LONICERA CAPRIFOLIUM FLOWER - UNII:5N1WD9784U) LONICERA CAPRIFOLIUM FLOWER1.42 g  in 3 g
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN0.07 g  in 3 g
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE0.00525 g  in 3 g
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73442-0013-13 g in 1 POUCH; Type 0: Not a Combination Product09/16/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/16/2020
    Labeler - I World Pharmaceutical Co., Ltd. (688222857)
    Registrant - I World Pharmaceutical Co., Ltd. (688222857)
    Establishment
    NameAddressID/FEIBusiness Operations
    I World Pharmaceutical Co., Ltd688222857manufacture(73442-0013)