La Roche Posay Laboratoire Dermatologique

Product NDC: 49967-907
11-digit product format: 499670907
Labeler code: 49967
Product ID: 49967-907_93f2cacd-67af-4ad8-9e0a-4de8330f808f
Type: HUMAN OTC DRUG
Nonproprietary name: Titanium dioxide and Zinc oxide
Dosage form: LOTION
Route: TOPICAL
Labeler: L'Oreal USA Products Inc
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2011-07-01
Substance: TITANIUM DIOXIDE; ZINC OXIDE
Active strength: 60; 50 mg/mL; mg/mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	49967-907	49967-907-02	D	Discontinued by firm		2026-11-13

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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

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: La Roche Posay Laboratoire Dermatologique
Brand name suffix: Anthelios 50 Mineral Ultra Light Sunscreen
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
TITANIUM DIOXIDE	60 mg/mL
ZINC OXIDE	50 mg/mL

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
SOI2LOH54Z	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
2ce83dc2-84b6-43fd-8b11-495d41cebc22	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
49967-907-01	La Roche Posay Laboratoire DermatologiqueAnthelios 50 Mineral Ultra Light Sunscreen	50 mL in 1 BOTTLE, PLASTIC	LOTION	50	17
49967-907-01	La Roche Posay Laboratoire DermatologiqueAnthelios 50 Mineral Ultra Light Sunscreen	1 in 1 CARTON	LOTION	1	17
49967-907-02	La Roche Posay Laboratoire DermatologiqueAnthelios 50 Mineral Ultra Light Sunscreen	3 mL in 1 TUBE	LOTION	3	17
49967-907-02	La Roche Posay Laboratoire DermatologiqueAnthelios 50 Mineral Ultra Light Sunscreen	1 in 1 CARTON	LOTION	1	17
49967-907-03	La Roche Posay Laboratoire DermatologiqueAnthelios 50 Mineral Ultra Light Sunscreen	5 mL in 1 TUBE	LOTION	5	17
49967-907-03	La Roche Posay Laboratoire DermatologiqueAnthelios 50 Mineral Ultra Light Sunscreen	1 in 1 CARTON	LOTION	1	17

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Titanium dioxide	ACTIVE INGREDIENT	15FIX9V2JP	LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS 50 MINERAL ULTRA LIGHT SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC]	7
Zinc oxide	ACTIVE INGREDIENT	SOI2LOH54Z	LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS 50 MINERAL ULTRA LIGHT SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC]	7
Titanium dioxide	ACTIVE MOIETY	15FIX9V2JP	LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS 50 MINERAL ULTRA LIGHT SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC]	7
Zinc oxide	ACTIVE MOIETY	SOI2LOH54Z	LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS 50 MINERAL ULTRA LIGHT SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC]	7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49967-907	LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS 50 MINERAL ULTRA LIGHT SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC]	17	Current NDC, Legacy NDC, 6 package rows	20231214_2ce83dc2-84b6-43fd-8b11-495d41cebc22.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 231 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Proceuticals Private Label by TiZO Tinted Facial Mineral Sunscreen Backbar	TITANIUM DIOXIDE, ZINC OXIDE	Fallien Cosmeceuticals, LTD	2be9f92a-a041-0595-e063-6394a90af7a8	2025-01-17	Warnings	Exact identifier application number: M020
Prequel Sun Barrier Mineral Sunscreen Broad Spectrum SPF 50	MINERAL SUNSCREEN	The Center Brands, LLC	cd35ae20-d5b7-479d-8a5e-0278eae9e83c	2025-01-17	Warnings	Exact identifier application number: M020
HUTTON KLEIN HK DERMATOLOGISTS SPF 40 Mineral Based Facial Sunscreen Tinted	TITANIUM DIOXIDE, ZINC OXIDE	Hutton, Kathleen MD	293a6a6c-adf3-452d-92f5-3baceb619e39	2025-01-16	Warnings	Exact identifier application number: M020
CAPTURE DREAMSKIN FRESH AND PERFECT CUSHION WITH SUNSCREEN BROAD SPECTRUM SPF 50 020	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	Parfums Christian Dior	594982d5-b4bf-4889-99b7-b3cd58fa8031	2025-01-16	Warnings	Exact identifier application number: M020
CAPTURE DREAMSKIN FRESH AND PERFECT CUSHION WITH SUNSCREEN BROAD SPECTRUM SPF 50 010	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	Parfums Christian Dior	26f1dcde-209e-4c6d-9577-1f3d3e21595f	2025-01-16	Warnings	Exact identifier application number: M020
CAPTURE DREAMSKIN FRESH AND PERFECT CUSHION WITH SUNSCREEN BROAD SPECTRUM SPF 50 000	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	Parfums Christian Dior	adba288c-e94f-4b26-8f7d-336f3e5108bd	2025-01-16	Warnings	Exact identifier application number: M020
Dolce and Gabbana Meet Your Flawless Matte Skin Duo	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Socoplan	3541c41b-f114-4734-a66f-be309ca6f3bf	2025-01-16	Warnings	Exact identifier application number: M020
SUNSTATION USA SPF-30 SPORT SUNSCREEN-	SUNSTATION USA SPF-30 SPORT SUNSCREEN-	Sunstation USA, LLC	2bd84b92-dcf0-404f-e063-6294a90a1060	2025-01-16		Exact identifier application number: M020
Snap On Racing Sunscreen Kit	AVOBENZONE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE	Greater Pacific Industries, Inc.	9f4f91d0-0fc5-43a3-be79-afce5afa2f95	2025-01-16	Warnings	Exact identifier application number: M020
Emme Diane Pure Protection Tinted Antioxidant Sunscreen	ZINC OXIDE	Emme Diane, Inc.	b2b4daf5-765b-426d-8a72-9278f7cd43d7	2025-01-16	Warnings	Exact identifier application number: M020
Emme Diane Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Emme Diane, Inc	ab53ad98-b667-4447-8177-724dbf771e80	2025-01-16	Warnings	Exact identifier application number: M020
Mineral Lip Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Hutton, Kathleen MD	2be51fdf-c3f2-463b-8c7d-bda07db17e1b	2025-01-16	Warnings	Exact identifier application number: M020
Sunny Sailor Captain s Classic Clear Mineral Sunscreen SPF 40	ZINC OXIDE	SUNNY SAILOR LLC	14ea2d11-c425-45d8-a23a-d4ed82a6439c	2025-01-15	Warnings	Exact identifier application number: M020
glo SKIN BEAUTY Oil-Free Tinted Primer SPF 30	GLO SKIN BEAUTY OIL-FREE TINTED PRIMER SPF 30	Hayden Caleel LLC	00bf7331-c9dc-4a8a-9ff3-901e0d07eac6	2025-01-15	Warnings	Exact identifier application number: M020
Black Girl Sunscreen Sunscreen SPF 30 Broad Spectrum	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	Black Girl Sunscreen, LLC	2bc42f6f-4eaf-fa28-e063-6294a90a93fb	2025-01-15	Warnings	Exact identifier application number: M020
Black Girl Sunscreen SPF 50 Broad Spectrum	HOMOSALATE, OCTOCRYLENE, OCTISALATE, ZINC OXIDE	Black Girl Sunscreen, LLC	2bc419b3-4de2-7ed9-e063-6394a90a255f	2025-01-15	Warnings	Exact identifier application number: M020
Black Girl Sunscreen SPF 45	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Black Girl Sunscreen, LLC	2bc47bd0-d81b-f1b9-e063-6394a90ad375	2025-01-15	Warnings	Exact identifier application number: M020
Black Girl Sunscreen SPF 50	OCTOCRYLENE, OCTISALATE, HOMOSALATE, AVOBENZONE	Black Girl Sunscreen, LLC	2bc46854-fe67-782b-e063-6294a90a79af	2025-01-15	Warnings	Exact identifier application number: M020
Black Girl Sunscreen SPF 50 broad Spectrum	AVOBENZONE, HOMOSALATE, OCTISALATE	Black Girl Sunscreen, LLC	2bc471f0-c93e-0c51-e063-6394a90a77f0	2025-01-15	Warnings	Exact identifier application number: M020
Black Girl Sunscreen SPF 45	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Black Girl Sunscreen, LLC	2bc4b1b1-5f19-7ba3-e063-6394a90a5de7	2025-01-15	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
15FIX9V2JP	TITANIUM DIOXIDE	13463-67-7	TITANIUM DIOXIDE
SOI2LOH54Z	ZINC OXIDE	1314-13-2	ZINC OXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49967-907-01	49967090701	1 BOTTLE, PLASTIC in 1 CARTON (49967-907-01) / 50 mL in 1 BOTTLE, PLASTIC		2011-07-01	0000-00-00	No	No	Current
49967-907-02	49967090702	1 TUBE in 1 CARTON (49967-907-02) > 3 mL in 1 TUBE	1 tube	2011-07-01	0000-00-00	No	No	Current
49967-907-03	49967090703	1 TUBE in 1 CARTON (49967-907-03) / 5 mL in 1 TUBE	1 tube	2019-12-02	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts	L'Oreal USA Products Inc \| Cosmetique Active Production \| Interspray	2023-12-13	HUMAN OTC DRUG LABEL	17