OHUI WHITE EXTREME ILLUMINATING PACT NO.10- titanium dioxide, octinoxate, arbutin, atractylodes japonica root oil powder

OHUI White Extreme Illuminating Pact No.10 by

Drug Labeling and Warnings

OHUI White Extreme Illuminating Pact No.10 by is a Otc medication manufactured, distributed, or labeled by LG Household and Healthcare, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 #20

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: 53208-534
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: 53208-534-02	1 in 1 BOX
1	NDC: 53208-534-01	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