Label: OUHI CELL POWER NO 1 ESSENCE- niacinamide, hydroxyproline liquid

  • Category: HUMAN OTC DRUG LABEL

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 6, 2010

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    NIACINAMIDE 2%

    HYDROXYPROLINE 0.5%

  • PURPOSE

    Wrinkle/Whitening functional cosmetic.

  • WARNINGS

    Stop use if rash or irritation develops and lasts.

  • WHEN USING

    Keep out of eyes. Rinse with water to remove.

  • INDICATIONS & USAGE

    Apply in the morning and evening after facial cleansing. Pump 1~2 times on your hand. Absorb in the essence by gently smoothing over your face with your fingertips along your face texture.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. Is swallowed, get medical help or contact a Poison Control Center right away.

  • INACTIVE INGREDIENT

    WATER, DIPROPYLENE GLYCOL, ALCOHOL, GLYCERETH-26, GLYCERIN, FRUIT, BIOSACCHARIDE GUM-1, METHYL GLUCETH-20, FILIPENDULA ULMARIA ROOT, YEAST, CETOSTEARYL ALCOHOL, TROMETHAMINE, EDETATE TRISODIUM, GERANIUM MACULATUM ROOT, PAEONIA LACTIFLORA ROOT, POLYDATIN.
  • DOSAGE & ADMINISTRATION

    Use before the Skin or Toner.

  • PRINCIPAL DISPLAY PANEL

    OHUI

     CELL POWER NO.1

     ESSENCE

    Cell Power No One Update


  • INGREDIENTS AND APPEARANCE
    OUHI CELL POWER NO 1 ESSENCE 
    niacinamide, hydroxyproline liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53208-491
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 mL  in 100 mL
    HYDROXYPROLINE (UNII: RMB44WO89X) (HYDROXYPROLINE - UNII:RMB44WO89X) HYDROXYPROLINE0.5 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERETH-26 (UNII: NNE56F2N14)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    FRUIT (UNII: C2AIY4ERZC)  
    BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)  
    METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
    FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS)  
    YEAST (UNII: 3NY3SM6B8U)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    TROMETHAMINE (UNII: 023C2WHX2V)  
    EDETATE TRISODIUM (UNII: 420IP921MB)  
    GERANIUM MACULATUM ROOT (UNII: 93IXI5B6OJ)  
    PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)  
    POLYDATIN (UNII: XM261C37CQ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53208-491-021 in 1 BOX
    1NDC:53208-491-0135 mL in 1 CONTAINER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/03/2010
    Labeler - LG Household and Healthcare, Inc. (688276187)
    Registrant - LG Household and Healthcare, Inc. (688276187)
    Establishment
    NameAddressID/FEIBusiness Operations
    LG Household and Healthcare, Inc.688276187manufacture