SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E

Product NDC: 58411-331
11-digit product format: 584110331
Labeler code: 58411
Product ID: 58411-331_47aac3f6-8b7d-10fb-e063-6394a90aafa0
Type: HUMAN OTC DRUG
Nonproprietary name: OCTINOXATE
Dosage form: CREAM
Route: TOPICAL
Labeler: SHISEIDO AMERICAS CORPORATION
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2017-08-01
Substance: OCTINOXATE
Active strength: 1832 mg/30mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E
Brand name suffix: Golden 3
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTINOXATE	1832 mg/30mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4Y5P7MUD51	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
8a9294c2-3933-4f9c-b7e6-1f446f441a16	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
5dbf91a8-ec29-4ffc-807c-e3bae7fb67b1	Product name	1	20201123
85bed648-23ca-4804-98e6-e36aee999cad	Product name	1	20190717
80de93b4-8a94-428d-beb7-d644353ee70b	Product name	1	20180424
eb4f7d5b-1286-40dc-b8bf-ad87ff51c688	Product name	1	20170522
db8eb201-78c7-4590-8a71-fac0a539bd8c	Product name	1	20170404
141092be-5eb5-452e-9f69-2d350aa70a87	Product name	1	20161208

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58411-331-50	SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION EGolden 3	30 mL in 1 JAR	CREAM	30		4
58411-331-50	SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION EGolden 3	1 in 1 CARTON	CREAM	1		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58411-331	SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E GOLDEN 1 (OCTINOXATE) CREAM SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E GOLDEN 2 (OCTINOXATE) CREAM SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E GOLDEN 3 (OCTINOXATE) CREAM SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E GOLDEN 4 (OCTINOXATE) CREAM SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E NEUTRAL 1 (OCTINOXATE) CREAM SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E NEUTRAL 2 (OCTINOXATE) CREAM SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E NEUTRAL 3 (OCTINOXATE) CREAM SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E NEUTRAL 4 (OCTINOXATE) CREAM SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E ROSE 2 (OCTINOXATE) CREAM SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E ROSE 3 (OCTINOXATE) CREAM SHISEIDO FUTURE LX TOTAL RADIANCE FOUNDATION E ROSE 4 (OCTINOXATE) CREAM [SHISEIDO AMERICAS CORPORATION]	3	Current NDC, Legacy NDC, 2 package rows	20241228_8a9294c2-3933-4f9c-b7e6-1f446f441a16.zip

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 156 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ATTITUDE Sensitive natural Mineral Sunscreen Stick SPF 50 Unscented	ZINC OXIDE	9055-7588 Qubec Inc.DBA ATTITUDE	4495a302-51b9-3bf2-e063-6294a90a7e4f	2025-11-28	Warnings	Exact identifier application number: M020
ATTITUDE Sunly Kids Mineral sunscreen Sprayer SPF 50 Watermelon and coco	ZINC OXIDE	9055-7588 Qubec Inc.DBA ATTITUDE	44aa1349-e3f1-9b80-e063-6294a90a0fbd	2025-11-28	Warnings	Exact identifier application number: M020
ATTITUDE Sunly Mineral sunscreen SPF 50 Unscented	ZINC OXIDE	9055-7588 Qubec Inc.DBA ATTITUDE	44aaa3c8-ccc4-ae93-e063-6394a90aedc5	2025-11-28	Warnings	Exact identifier application number: M020
ATTITUDE Sunly Baby Mineral sunscreen SPF 50 Unscented	ZINC OXIDE	9055-7588 Qubec Inc.DBA ATTITUDE	44aba591-04da-fe09-e063-6394a90a912a	2025-11-28	Warnings	Exact identifier application number: M020
ATTITUDE Sunly Kids Mineral sunscreen SPF 50 Unscented	ZINC OXIDE	9055-7588 Qubec Inc.DBA ATTITUDE	44aba6d7-7989-0637-e063-6394a90a6c8f	2025-11-28	Warnings	Exact identifier application number: M020
ATTITUDE Sunly Mineral sunscreen SPF 50 Tropical coco	ZINC OXIDE	9055-7588 Qubec Inc.DBA ATTITUDE	44abca13-8ba9-8925-e063-6294a90accb5	2025-11-28	Warnings	Exact identifier application number: M020
ATTITUDE Sensitive natural baby Mineral sunscreen SPF 50 Unscented	ZINC OXIDE	9055-7588 Qubec Inc.DBA ATTITUDE	44abdfe1-ea6b-a158-e063-6294a90a3eb8	2025-11-28	Warnings	Exact identifier application number: M020
ATTITUDE Sunly Kids Mineral sunscreen SPF 50 Watermelon and coco	ZINC OXIDE	9055-7588 Qubec Inc.DBA ATTITUDE	44aca1d5-6e0a-def3-e063-6294a90aca26	2025-11-28	Warnings	Exact identifier application number: M020
ATTITUDE Sunly Mineral sunscreen SPF 50 Sun kissed vanilla	ZINC OXIDE	9055-7588 Qubec Inc.DBA ATTITUDE	44aca181-2a90-20a6-e063-6394a90aff47	2025-11-28	Warnings	Exact identifier application number: M020
ATTITUDE Sunly Mineral sunscreen Sprayer SPF 50 Sun kissed vanilla	ZINC OXIDE	9055-7588 Qubec Inc.DBA ATTITUDE	44aa529b-2077-3660-e063-6394a90aa405	2025-11-28	Warnings	Exact identifier application number: M020
ATTITUDE Sunly Lip Balm SPF 15 Unscented	ZINC OXIDE	9055-7588 Qubec Inc.DBA ATTITUDE	44ad65f0-ec1d-1638-e063-6294a90a2244	2025-11-28	Warnings	Exact identifier application number: M020
HOEGOA Hair Scalp Sunscreen Mineral	TITANIUM DIOXIDE	Guangzhou Hoegoa Biotechnology Co., Ltd.	44b37930-b302-338c-e063-6394a90a5f7f	2025-11-28	Warnings	Exact identifier application number: M020
OCEAURA Glitter Sunscreen	TITANIUM DIOXIDE	Guangzhou Oceaura Biotechnology Co., Ltd.	44b47284-57cd-2e61-e063-6394a90a5072	2025-11-28	Warnings	Exact identifier application number: M020
OUHOE Moisturizing And Translucent Sunscreen	TITANIUM DIOXIDE	Shantou Ouhoe Technology Co., Ltd.	34e8e4a6-2782-9a3d-e063-6394a90a84c2	2025-11-27	Warnings	Exact identifier application number: M020
OUHOE Protection Sunscreen	TITANIUM DIOXIDE	Shantou Ouhoe Technology Co., Ltd.	4272dcef-eda5-1013-e063-6294a90adf38	2025-11-27	Warnings	Exact identifier application number: M020
OUHOE Sunscreen	TITANIUM DIOXIDE	Shantou Ouhoe Technology Co., Ltd.	42fcc9ed-083c-6582-e063-6394a90ae9e6	2025-11-27	Warnings	Exact identifier application number: M020
EELHOE Sun Cream	TITANIUM DIOXIDE	Shantou Eelhoe Daily Chemical Technology Co., Ltd.	305cb87e-450f-840a-e063-6294a90a883f	2025-11-27	Warnings	Exact identifier application number: M020
EELHOE Bio Sun Stick	TITANIUM DIOXIDE	Shantou Eelhoe Daily Chemical Technology Co., Ltd.	349a3d72-9969-855d-e063-6394a90a281c	2025-11-27	Warnings	Exact identifier application number: M020
EELHOE Cica Cooling Sun Stick	TITANIUM DIOXIDE	Shantou Eelhoe Daily Chemical Technology Co., Ltd.	305c13af-0843-f478-e063-6394a90a42de	2025-11-27	Warnings	Exact identifier application number: M020
EELHOE Quick Sun Stick Protection Bar	TITANIUM DIOXIDE	Shantou Eelhoe Daily Chemical Technology Co., Ltd.	3578c958-a457-402b-e063-6394a90a7342	2025-11-27	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
58411-331-50	58411033150	1 JAR in 1 CARTON (58411-331-50) / 30 mL in 1 JAR	1 jar	2017-08-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
SHISEIDO FUTURE SOLUTION LX TOTAL RADIANCE FOUNDATION E	SHISEIDO AMERICAS CORPORATION \| Shiseido America Inc.	2026-01-05	HUMAN OTC DRUG LABEL	4