OHUI SUNSCIENCE LUMINOUS WHITENING SUNBLOCK description, usages, side effects, indications, overdosage, supplying and lots more!

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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

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


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