Label: KIMITE- scopolamine patch, extended release

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated December 12, 2018

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  • ACTIVE INGREDIENT

    Scopolamine

  • PURPOSE

    Relieve the vomiting, nausea, dizziness, anorexia, and other symptoms resulted from sickness of cars, ships, airplanes, trains and other means of transport

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    ■ Tear the protective layer, adhere the adhesive layer to the navel or the back of your ears

    ■ One/ Two patch per time, accoding to your body condition

    ■ Attach 10 minutes before the travel, the effect will last about 1-3 days

  • WARNINGS

    ■ Avoid use on allergic and broken skin

    ■ Not use by pregnant women kid under aged 4

    ■ Not recommend to use by poorly surgery body

  • INACTIVE INGREDIENT

    The abstract of salflower, tall gastrodia tuber, sanchi, hairy datura flower, pinellia tuber, obtuseleaf cinnamon bark, frankincense, dahurian angelica root, bomeol

  • DOSAGE & ADMINISTRATION

    For external use only

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    KIMITE 
    scopolamine patch, extended release
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72689-0023
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SCOPOLAMINE (UNII: DL48G20X8X) (SCOPOLAMINE - UNII:DL48G20X8X) SCOPOLAMINE1.5 mg
    Inactive Ingredients
    Ingredient NameStrength
    DATURA FEROX WHOLE (UNII: NY0VWX7OX1)  
    FRANKINCENSE (UNII: R9XLF1R1WM)  
    ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)  
    PINELLIA TERNATA WHOLE (UNII: 71T2LKP8GL)  
    GASTRODIA ELATA TUBER (UNII: 08F85I5YAV)  
    PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72689-0023-12 in 1 BOX; Type 0: Not a Combination Product11/16/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/15/2018
    Labeler - OASIS TRADING (689991468)
    Registrant - OASIS TRADING (689991468)
    Establishment
    NameAddressID/FEIBusiness Operations
    OASIS TRADING689991468manufacture(72689-0023)
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