SHISEIDO WHITE LUCENT- octinoxate and octocrylene emulsion

SHISEIDO WHITE LUCENT by

Drug Labeling and Warnings

SHISEIDO WHITE LUCENT by is a Otc medication manufactured, distributed, or labeled by SHISEIDO AMERICA INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

• Active ingredients: Purpose
• OCTINOXATE 4.9%: Sunscreen
• OCTOCRYLENE 5.0%: Sunscreen

Uses

• helps prevent sunburn
• higher SPF gives more sunburn protection

Warnings

For external use only

When using this product

• keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

• rash or irritation develops and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• apply smoothly to face before sun exposure and as needed.
• children under 6 months of age: ask a doctor.

Inactive ingredients

WATER, GLYCERIN, DIPROPYLENE GLYCOL, SD ALCOHOL 40-B, DIMETHICONE, SILICA, DIISOPROPYL SEBACATE, TRANEXAMIC ACID, HYDROGENATED POLYISOBUTENE, EUPHORBIA CERIFERA (CANDELILLA) WAX, PEG/PPG-14/7 DIMETHYL ETHER, ERYTHRITOL, PEG/PPG-17/4 DIMETHYL ETHER, 2-O-ETHYL ASCORBIC ACID, XANTHAN GUM GLUCOSYL HESPERIDIN, PHYTOSTERYL/OCTYLDODECYL LAUROYL GLUTAMATE, SODIUM HYALURONATE, BUTYL METHOXYDIBENZOYLMETHANE PEG/PPG-19/19 DIMETHICONE, BEHENYL ALCOHOL, PPG-8-CETETH-20, BEHENETH-20, TRISODIUM EDTA, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, CARBOMER, STEARYL ALCOHOL, POTASSIUM HYDROXIDE, HYDROXYPROPYLCELLULOSE, BHT, POLYSILICONE-2, SODIUM METABISULFITE, TOCOPHEROL, PHENOXYETHANOL, FRAGRANCE, TITANIUM DIOXIDE, IRON OXIDES

Questions?

1-800-906-7503

SPL UNCLASSIFIED SECTION

SHISEIDO AMERICA INC.
NEW YORK, N.Y. 10022
MADE IN U.S.A.
SHISEIDO DIST.
NEW YORK PARIS MILANO
GLO. 10393

www.shiseido.com

PRINCIPAL DISPLAY PANEL - 75 mL Carton

SHISEIDO

WHITE LUCENT

Brightening
Protective Emulsion w
SPF 15 PA++
SUNSCREEN

75mL 2.5 FL. OZ.

INGREDIENTS AND APPEARANCE

SHISEIDO WHITE LUCENT 
octinoxate and octocrylene emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52686-228
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	3.479 g  in 71 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	3.55 g  in 71 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52686-228-10	1 in 1 CARTON	02/01/2010
1		71 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	02/01/2010

Labeler - SHISEIDO AMERICA INC. (782677132)

Establishment
Name	Address	ID/FEI	Business Operations
SHISEIDO AMERICA INC.		782677132	analysis(52686-228) , manufacture(52686-228)