Label: OKYONGSOO- nardostachys chinensis whole liquid

  • 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 June 18, 2012

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  • ACTIVE INGREDIENT

    active ingredient: NARDOSTACHYS CHINENSIS WHOLE
  • INACTIVE INGREDIENT

    inactive ingredient:  purified water, lemon extract, baizhi extract, lysimachia foenum graecum, jujube extract, mother chrysanthemum extract, opuntia extract, metaplexis japonica, benincasis cerifera, citric acid, perfume, pigment
  • PURPOSE

    skin protectant (anti-wrinkle)
  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children
  • INDICATIONS & USAGE

    - apply only for skin
    - apply 2 or 3 times a day
    - massage with your finger over 2 min and let them dry


  • WARNINGS

    - keep out of eyes, ears and mouth
    - if contact occurs, rinse away with plenty of cold water
  • DOSAGE & ADMINISTRATION

    - for external use only
  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    OKYONGSOO 
    nardostachys chinensis whole liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50973-1001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NARDOSTACHYS CHINENSIS WHOLE (UNII: FJ4AE60Q9V) (NARDOSTACHYS CHINENSIS WHOLE - UNII:FJ4AE60Q9V) NARDOSTACHYS CHINENSIS WHOLE1 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    JUJUBE FRUIT (UNII: G55HNL2C70)  
    CHRYSANTHEMUM X MORIFOLIUM FLOWER (UNII: 2GR3C1A0WV)  
    HALIMEDA OPUNTIA (UNII: 5KM10205ZI)  
    ASCLEPIAS QUADRIFOLIA WHOLE (UNII: X01T4I85QG)  
    BENINCASA HISPIDA FRUIT (UNII: 66L2YSO9UG)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50973-1001-150 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/18/2012
    Labeler - Woori Health Promotion Town (557817062)
    Registrant - Woori Health Promotion Town (557817062)
    Establishment
    NameAddressID/FEIBusiness Operations
    Woori Health Promotion Town557817062manufacture