SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM

Product NDC: 58411-296
11-digit product format: 584110296
Labeler code: 58411
Product ID: 58411-296_47aab51b-96c9-d1c1-e063-6294a90a738e
Type: HUMAN OTC DRUG
Nonproprietary name: OCTINOXATE and TITANIUM DIOXIDE
Dosage form: CREAM
Route: TOPICAL
Labeler: SHISEIDO AMERICAS CORPORATION
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2017-02-01
Substance: OCTINOXATE; TITANIUM DIOXIDE
Active strength: 138; 123 mg/4mL; mg/4mL
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 18 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	58411-296-10	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	58411-296-10	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	58411-296-10	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	58411-296-10	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	58411-296-10	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	58411-296-10	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	58411-296-10	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	58411-296-10	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	58411-296-10	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

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 WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM
Brand name suffix: NATURAL LIGHT
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTINOXATE	138 mg/4mL
TITANIUM DIOXIDE	123 mg/4mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
15FIX9V2JP	Internal UNII lookup
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
bf736c5b-fc33-4cd5-8d18-03929f739d76	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d1c9d1af-bddd-448d-86f7-69052b7d5b47	Product name	1	20220627
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
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
58411-296-10	2026-01-06	C162847	48780-1	9d75b9d0-6be3-f424-e053-dadaa90a57ce	SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM
58411-296-10	2025-01-31	C162847	48780-1	9d75b9d0-6be3-f424-e053-dadaa90a57ce	SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58411-296-10	SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUMNATURAL LIGHT	4 mL in 1 BOTTLE	CREAM	4		4
58411-296-10	SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUMNATURAL LIGHT	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
58411-296	SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM NATURAL LIGHT (OCTINOXATE AND TITANIUM DIOXIDE) CREAM SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM NATURAL (OCTINOXATE AND TITANIUM DIOXIDE) CREAM SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM MEDIUM (OCTINOXATE AND TITANIUM DIOXIDE) CREAM [SHISEIDO AMERICAS CORPORATION]	3	Current NDC, Legacy NDC, 2 package rows	20231222_bf736c5b-fc33-4cd5-8d18-03929f739d76.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 67 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Touch in SOL No Poreblem Airbrushed Primer	OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE	BONNE Co., Ltd	4685ff24-0bb0-3502-e063-6394a90abfee	2026-01-29	Warnings	Exact identifier application number: M020
Sheer Touch Sunscreen SPF 70	AVOBENZONE, HOMOSALATE, OCTISALATE	Aldi, Inc	c7650d20-7cb9-4861-8a30-cf4a9cd424e9	2026-01-29	Warnings, Adverse reactions	Exact identifier application number: M020
Sunscreen SPF 70	AVOBENZONE, HOMOSALATE, OCTISALATE	Aldi, Inc	32c0613e-0f5a-47f5-b2f3-f32ae07cbc76	2026-01-29	Warnings, Adverse reactions	Exact identifier application number: M020
Vacation Original Coconut SPF 15	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	Vacation INC.	a9a0b558-b8e6-44ea-9b57-6938837a04fb	2026-01-29	Warnings	Exact identifier application number: M020
SHISEIDO SPORTS BB DARK	OCTINOXATE AND TITANIUM DIOXIDE	SHISEIDO AMERICAS CORPORATION	f4fc4b6a-9507-496e-9ecb-8400055ecf2d	2026-01-28	Warnings	Exact identifier application number: M020
Hampton Sun SPF 30 Mineral	ZINC OXIDE 7.20% TITANIUM DIOXIDE 4.00%	S&C Hampton Sun LLC	b8ee428e-07d3-4c6c-853c-cfbe3e4002d9	2026-01-28	Warnings	Exact identifier application number: M020
SHISEIDO FUTURE LX UNIVERSAL DEFENSE S	OCTISALATE, OCTOCRYLENE, AND ZINC OXIDE	SHISEIDO AMERICAS CORPORATION	0a6f8eef-48e9-44f5-9811-629bc0dc07d0	2026-01-28	Warnings	Exact identifier application number: M020
Hampton Sun SPF 45 Tinted Face	HOMOSALATE 10% OCTOCRYLENE 6% AVOBENZONE 3%	S&C Hampton Sun LLC	0fc0f2c7-ec0f-4976-9872-82a6bfe8b46b	2026-01-28	Warnings	Exact identifier application number: M020
Walgreens 70 Sport Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	49775d1a-e573-a596-e063-6294a90a7cf6	2026-01-28	Warnings	Exact identifier application number: M020
AVON ANEW ULTIMATE MULTI-PERFORMANCE DAY BROAD SPECTRUM SPF 25 SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTINOXATE, OXYBENZONE	The Avon Company	49784430-2ffe-0cbb-e063-6394a90adb23	2026-01-28	Warnings	Exact identifier application number: M020
ALOE UP SPORT SPF-50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Aloe Care International, LLC	3f2f90f1-28dd-48e8-9083-ea04815acc6b	2026-01-28	Warnings	Exact identifier application number: M020
ALOE UP PRO 30 CONTINUOUS SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE	Aloe Care International, LLC	baf32d84-4db5-4ed0-9814-5470b7d1f4a4	2026-01-28	Warnings	Exact identifier application number: M020
ALOE UP PRO 15	AVOBENZONE, OCTISALATE, OCTOCRYLENE	Aloe Care International, LLC	5b0f43fc-f4a6-4403-a40e-e0198a6f2ebd	2026-01-28	Warnings	Exact identifier application number: M020
ALOE UP PRO 50 CONTINUOUS SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE	Aloe Care International, LLC	dc33d9e8-3463-485d-a1ee-6319ed91454c	2026-01-28	Warnings	Exact identifier application number: M020
ALOE ICE SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE	Aloe Care International, LLC	e4b861d2-3680-4ed7-8650-d1d839da5ab2	2026-01-28	Warnings	Exact identifier application number: M020
ALOE UP SPORT SPF-15	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Aloe Care International, LLC	1bf1635a-825e-417f-97b4-4bce6d251d19	2026-01-28	Warnings	Exact identifier application number: M020
Mineral Sunscreen	ZINC OXIDE 20%	The Daily Suncare LLC, DBA Daily Shade	1a392f6b-1bb1-c49d-e063-6294a90a791d	2026-01-28	Warnings	Exact identifier application number: M020
KIZO LAB UV DEFENSE CLEAR SUNSCREN SPF50	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	YB CHEMIA LLC	0053ae49-b9a1-c3f4-e063-6394a90abcb8	2026-01-28	Warnings	Exact identifier application number: M020
Orange Gel	AVOBENZONE OCTISALATE OCTOCRYLENE HOMOSALATE	Vacation Inc.	132896ef-d6c6-4ec7-e063-6294a90a103b	2026-01-28	Warnings	Exact identifier application number: M020
REDEFINE Triple Defense	AVOBENZONE, OCTISALATE, OCTOCRYLENE	Rodan & Fields	d1dd62c6-33ac-4941-ab99-9eb8cc3c208a	2026-01-27	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
15FIX9V2JP	TITANIUM DIOXIDE	13463-67-7	TITANIUM DIOXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
58411-296-10	58411029610	1 BOTTLE in 1 CARTON (58411-296-10) / 4 mL in 1 BOTTLE	1 bottle	2017-02-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
SHISEIDO WHITE LUCENT ONMAKEUP SPOT CORRECTING SERUM	SHISEIDO AMERICAS CORPORATION \| SHISEIDO AMERICA INC.	2026-01-05	HUMAN OTC DRUG LABEL	4