Home > Drugs A-Z > OHUI White Extreme Illuminating Pact No.10

OHUI White Extreme Illuminating Pact No.10 (LG Household and Healthcare, Inc.)

Available Formats

Dosage Form Package Information Links
POWDER 1 CONTAINER in 1 BOX (53208-533-02) > 11 g in 1 CONTAINER (53208-533-01) Label Information

Complete OHUI White Extreme Illuminating Pact No.10 Information

  • ACTIVE INGREDIENT

    TITANIUM DIOXIDE          9.84%
    OCTINOXATE                  4.5%
    ARBUTIN                         2%
    ATRACTYLODES JAPONICA ROOT OIL     0.1%


  • WARNINGS AND PRECAUTIONS

    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.
  • WHEN USING

    Keep out of eyes. Rinse with water to remove
  • STOP USE

    Stop use if a rash or irritation develops and lasts.


  • PRINCIPAL DISPLAY PANEL

    OHUI White Extreme Illuminating Pact No.10
    OHUI White Extreme Illuminating Pact #10
  • INGREDIENTS AND APPEARANCE
    OHUI WHITE EXTREME ILLUMINATING PACT NO.10 
    titanium dioxide, octinoxate, arbutin, atractylodes japonica root oil powder
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:53208-533
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 9.84 g  in 100 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 4.5 g  in 100 g
    ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF) ARBUTIN 2 g  in 100 g
    ATRACTYLODES JAPONICA ROOT OIL (UNII: EC228KGY00) (ATRACTYLODES JAPONICA ROOT OIL - UNII:EC228KGY00) ATRACTYLODES JAPONICA ROOT OIL 0.1 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    TALC (UNII: 7SEV7J4R1U)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    BORON NITRIDE (UNII: 2U4T60A6YD)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    MICA (UNII: V8A1AW0880)  
    TALC (UNII: 7SEV7J4R1U)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    MAGNESIUM MYRISTATE (UNII: Z1917F0578)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    DIAMOND (UNII: 6GRV67N0U2)  
    COPPER (UNII: 789U1901C5)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:53208-533-02 1 in 1 BOX
    1 NDC:53208-533-01 11 g in 1 CONTAINER
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 05/25/2011
    Labeler - LG Household and Healthcare, Inc. (688276187)
    Registrant - LG Household and Healthcare, Inc. (688276187)
    Establishment
    Name Address ID/FEI Business Operations
    LG Household and Healthcare, Inc. 688276187 manufacture