Label: CHEONG RO HWAN- creosote pill

  • 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 13, 2018

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  • ACTIVE INGREDIENT

    creosote, phellodendron bark ext. powder, powdered geranium herb

  • PURPOSE

    ■ antidiarrhea

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    ■ children under 7 years of age: consult a doctor

    ■ take 1-2 tablet as symptoms accur, as directed by a doctor

  • WARNINGS

    Ask a doctor before use if you have taking a prescription drug. Antacids may interact with certain prescription drugs.

    When using this product

    ■ Do not take more than 4 pills in 24 hours

    ■ Do not use the maximum dosage for more than 1 weeks

    Keep out of the reach of children. This package contains enough drug to seriously harm a child

  • INACTIVE INGREDIENT

    starch, glucose

  • DOSAGE & ADMINISTRATION

    For oral use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CHEONG RO HWAN 
    creosote pill
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72689-0029
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WOOD CREOSOTE (UNII: 3JYG22FD73) (WOOD CREOSOTE - UNII:3JYG22FD73) WOOD CREOSOTE44.4 mg
    Inactive Ingredients
    Ingredient NameStrength
    SOYBEAN OIL (UNII: 241ATL177A)  
    STARCH, RICE (UNII: 4DGK8B7I3S)  
    Product Characteristics
    ColorblackScoreno score
    ShapeROUNDSize5mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72689-0029-1120 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product11/20/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/13/2018
    Labeler - OASIS TRADING (689991468)
    Registrant - OASIS TRADING (689991468)
    Establishment
    NameAddressID/FEIBusiness Operations
    OASIS TRADING689991468manufacture(72689-0029) , label(72689-0029)