SHISEIDO WHITE LUCENT

Manufacturer: SHISEIDO AMERICA INC.
Effective date: 2018-12-19
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-02 00:40:41

Label at a glance#

ProductSHISEIDO WHITE LUCENT

Active ingredientOCTINOXATE, OCTOCRYLENE

Label structure9 sections

Indications and uses

helps prevent sunburn higher SPF gives more sunburn protection

Dosage and administration

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

Contacts and useful links#

PhoneLabel contact1-800-906-7503

Websitewww.shiseido.com

www.shiseido.com

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

*Active ingredients*	*Purpose*
OCTINOXATE 4.9%	Sunscreen
OCTOCRYLENE 5.0%	Sunscreen

Uses

INDICATIONS & USAGE SECTION

helps prevent sunburn
higher SPF gives more sunburn protection

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash or irritation develops and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SHISEIDO

WHITE LUCENT

Brightening
Protective Emulsion w
SPF 15 • PA++
SUNSCREEN

75mL 2.5 FL. OZ.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52686-228-10	2023-09-27	C162847	48780-1	9d75b9d0-1507-f424-e053-dadaa90a57ce	SHISEIDO WHITE LUCENT BRIGHTENING PROTECTIVE EMULSION w SPF 15•PA++
52686-228-10	2020-01-31	C162847	48780-1	9d75b9d0-1507-f424-e053-dadaa90a57ce	SHISEIDO WHITE LUCENT BRIGHTENING PROTECTIVE EMULSION w SPF 15•PA++

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Octinoxate	ACTIVE INGREDIENT	4Y5P7MUD51	1
Octocrylene	ACTIVE INGREDIENT	5A68WGF6WM	1
Octinoxate	ACTIVE MOIETY	4Y5P7MUD51	1
Octocrylene	ACTIVE MOIETY	5A68WGF6WM	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

SHISEIDO WHITE LUCENT
Octinoxate and Octocrylene
OCTINOXATE
OCTOCRYLENE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52686-228	52686-228-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
OCTINOXATE	4Y5P7MUD51	ACTIB
OCTOCRYLENE	5A68WGF6WM	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0d6c1507-e4e1-43bb-ae3a-ba7cbe810f71			fcbe66ac-d73d-414b-bf26-f6a9eda2da3c	2023-09-27	Warnings	Exact identifier spl set id: fcbe66ac-d73d-414b-bf26-f6a9eda2da3c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.