Home – OHUI SUNSCIENCE LUMINOUS WHITENING SUNBLOCK

OHUI SUNSCIENCE LUMINOUS WHITENING SUNBLOCK

LG Household and Healthcare, Inc.
LG Household and Healthcare, Inc.

Drug Fact

FULL PRESCRIBING INFORMATION

Active ingredient

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.

OHUI SUNSCIENCE LUMINOUS WHITENING SUNBLOCK

ENSULIZOLE, OCTISALATE, BEMOTRIZINOL, OCTOCRYLENE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, ZINC OXIDE, TITANIUM DIOXIDE, ATRACTYLODES JAPONICA ROOT OIL CREAM

Product Information
Product Type	Human otc drug label	Item Code (Source)	NDC:53208-518
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Ensulizole Ensulizole		3.9 mL
OCTISALATE OCTISALATE		4.7 mL
BEMOTRIZINOL		1.5 mL
OCTOCRYLENE Octocrylene		5 mL
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE		1 mL
Zinc Oxide Zinc oxide		12.3 mL
titanium dioxide		3.67 mL
ATRACTYLODES JAPONICA ROOT OIL ATRACTYLODES JAPONICA ROOT OIL		0.525 mL

Inactive Ingredients
Ingredient Name	Strength
water
ALCOHOL
TROLAMINE
tromethamine
PANTHENOL
DIPROPYLENE GLYCOL
PONCIRUS TRIFOLIATA FRUIT
METHYLPARABEN
ETHYLPARABEN
MAGNESIUM SULFATE, UNSPECIFIED
CYCLOMETHICONE 5
HECTORITE
ZINC STEARATE
phenethyl benzoate
SILICON DIOXIDE
ISODODECANE

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC:53208-518-01	50 in 1 CONTAINER
2	NDC:53208-518-02	1 in 1 BOX

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
part	part352	2011-04-06

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!