Label: ISAKNOX X202 WHITENING SECRET ESSENCE- diosmetin cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated May 25, 2011

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  • ACTIVE INGREDIENT

    DIHYDROXYMETHOXYCHALCON 0.065

    DIOSMETIN 0.055%
  • WARNINGS

    For external use only.

  • 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.

  • PURPOSE

    Whitening functional cosmetic.

  • WHEN USING

    Keep out of eyes. Rinse with water to remove.

  • INDICATIONS & USAGE

    After applying toner, dispense 2-3 amounts and apply gently evenly onto your cheeks, chin, nose, and forehead.

  • INACTIVE INGREDIENT

    WATER, DIPROPYLENE GLYCOL, TRIETHYLHEXANOIN, GLYCERIN, DOCOSANOL, POLYETHYLENE GLYCOL 400, CETOSTEARYL ALCOHOL, CYCLOMETHICONE 5, ALCOHOL, PONCIRUS TRIFOLIATA FRUIT, BETAINE, DIMETHICONE, METHYLPARABEN, TROMETHAMINE, GLYCERYL MONOSTEARATE, PROPYLPARABEN, ETHYLPARABEN, EDETATE TRISODIUM, NIACINAMIDE, PAEONIA LACTIFLORA ROOT, CANNA INDICA ROOT.
  • DOSAGE & ADMINISTRATION

    The Secret-Kit tm capsules, comprising active whitening ingredients and fine whine particles, will burst as the essence gets absorbed, transforming your dull, lifeless complexion into more pure and transparent skin.

  • PRINCIPAL DISPLAY PANEL

    IK X2D2 Whitening Secret Essence
  • INGREDIENTS AND APPEARANCE
    ISAKNOX X202 WHITENING SECRET ESSENCE 
    diosmetin cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53208-531
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIOSMETIN (UNII: TWZ37241OT) (DIOSMETIN - UNII:TWZ37241OT) DIOSMETIN0.055 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    PONCIRUS TRIFOLIATA FRUIT (UNII: 44445L49J2)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    EDETATE TRISODIUM (UNII: 420IP921MB)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)  
    CANNA INDICA ROOT (UNII: BZK836AQFQ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53208-531-021 in 1 BOX
    1NDC:53208-531-0150 mL in 1 CONTAINER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/01/2011
    Labeler - LG Household and Healthcare, Inc. (688276187)
    Registrant - LG Household and Healthcare, Inc. (688276187)
    Establishment
    NameAddressID/FEIBusiness Operations
    LG Household and Healthcare, Inc.688276187manufacture
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