OHUI WHITE EXTREME ILLUMINATING PACT NO.10 - titanium dioxide, octinoxate, arbutin, atractylodes japonica root oil powder 
LG Household and Healthcare, Inc.

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.

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Drug Fact

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

For external use only

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

Keep out of eyes. Rinse with water to remove

Stop use if a rash or irritation develops and lasts.

OHUI White Extreme Illuminating Pact No.20
OHUI White Extreme Illuminating Pact #20
OHUI WHITE EXTREME ILLUMINATING PACT NO.10 
titanium dioxide, octinoxate, arbutin, atractylodes japonica root oil powder
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53208-534
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE9.84 g  in 100 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE4.5 g  in 100 g
ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF) ARBUTIN2 g  in 100 g
ATRACTYLODES JAPONICA ROOT OIL (UNII: EC228KGY00) (ATRACTYLODES JAPONICA ROOT OIL - UNII:EC228KGY00) ATRACTYLODES JAPONICA ROOT OIL0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53208-534-021 in 1 BOX
1NDC:53208-534-0111 g in 1 CONTAINER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35205/25/2011
Labeler - LG Household and Healthcare, Inc. (688276187)
Registrant - LG Household and Healthcare, Inc. (688276187)
Establishment
NameAddressID/FEIBusiness Operations
LG Household and Healthcare, Inc.688276187manufacture

Revised: 5/2011
Document Id: 6c06b338-5bcc-4743-a8a2-646827541f11
Set id: 089727e5-b273-4872-9a10-093a342756a2
Version: 1
Effective Time: 20110525
 
LG Household and Healthcare, Inc.