Label: YEO DANBI- glycerin liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated October 17, 2014

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  • ACTIVE INGREDIENT

    glycerin


  • INACTIVE INGREDIENT

    black bean ext, colloidal silver, iris ext etc


  • PURPOSE

    for itching skin
    skin protectant


  • KEEP OUT OF REACH OF CHILDREN

    keep out or reach of the children


  • INDICATIONS & USAGE

    After spraying it 2 or 3 times into sanitary pads, Please wear it.

  • WARNINGS

    Do not splash it directly to the skin.If you splash it directly to the skin, you feel tingling because of sterilizing effect.The symptoms will clear up after 20 or 30 seconds.

  • DOSAGE & ADMINISTRATION

    for exernal use only


  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    YEO DANBI 
    glycerin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69224-3001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69224-3001-130 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34710/17/2014
    Labeler - GL BioTech (689057539)
    Registrant - GL BioTech (689057539)
    Establishment
    NameAddressID/FEIBusiness Operations
    GL BioTech 689057539manufacture(69224-3001)
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