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 278 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Equate Sunscreen SPORT SPF 100	AVOBENZONE HOMOSALATE OCTISALATE OCTOCRYLENE OXYBENZONE	Walmart Stores Inc.	4fc58cea-082a-4535-9c51-8e7dedc15be3	2024-10-16	Warnings	Exact identifier application number: M020
Equate Sunscreen SPF 50 KIDS Broad Spectrum	TITANIUM DIOXIDE, ZINC OXIDE	WAL-MART STORES INC	81cb6b2e-1ca3-4a83-a8df-9bfee61e79af	2024-10-16	Warnings	Exact identifier application number: M020
Equate Sunscreen SPF100 SPORT Broad Spectrum	AVOBENZONE HOMOSALATE OCTISALATE OCTOCRYLENE OXYBENZONE	WAL-MART STORES INC	1ce4839b-f693-4653-8fe2-444df76eb83c	2024-10-16	Warnings	Exact identifier application number: M020
Equate Sunscreen Mineral Based KIDS Broad Spectrum spf 50	HOMOSALATE , OCTOCRYLENE, ZINC OXIDE	Wal-Mart Stores Inc	0cdfc3a1-4bfa-474d-a4eb-4bfa1e628c89	2024-10-16	Warnings	Exact identifier application number: M020
EQUATE Sunscreen BABY Broad Spectrum SPF 50	AVOBENZONE HOMOSALATE OCTOCRYLENE	WAL-MART STORES INC	b2083cbd-ef19-4edc-9d7d-eca3452ee0ee	2024-10-16	Warnings	Exact identifier application number: M020
Equate-Sunscreen Broad Spectrum SPF 50 ULTRA	AVOBENZONE HOMOSALATE OCTISALATE OCTOCRYLENE	Wal-Mart Stores Inc	bbe06f23-0d0f-43ff-9d1b-37a99d9d6206	2024-10-16	Warnings	Exact identifier application number: M020
BIG LOTS SOUNDBODY SPF 50 SPORT SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	BIG LOTS STORES, INC.	c8c1c904-12f5-48e0-e053-2a95a90a9f75	2024-10-16	Warnings	Exact identifier application number: M020
Big Lots Soundbody SPF 70 Sport Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTCRYLENE	BIG LOTS STORES, INC.	e717ec77-8beb-645a-e053-2a95a90ac11b	2024-10-16	Warnings	Exact identifier application number: M020
Big Lots Soundbody SPF 50 Ultra Sport Sunscreen	AVOBENZONE, HOMOSALATE, OCTOCRYLENE	BIG LOTS STORES, INC.	f0dcb5d8-a3e5-4334-e053-2995a90a535a	2024-10-16	Warnings	Exact identifier application number: M020
Big Lots Soundbody SPF 30 Sport Sunscreen	AVOBENZONE, HOMOSALATE, OCTOCRYLENE,	BIG LOTS STORES, INC.	c8aede4f-3d84-63d1-e053-2a95a90afb1a	2024-10-16	Warnings	Exact identifier application number: M020
Big Lots Soundbody SPF 70 Sun Defense	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE	BIG LOTS STORES, INC.	db3ad809-d6c9-6c83-e053-2a95a90ac58b	2024-10-16	Warnings	Exact identifier application number: M020
BIG LOTS SOUNDBODY KIDS SUNSCREEN SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	BIG LOTS STORES, INC.	e4b70fdb-7548-175c-e053-2995a90adfe6	2024-10-16	Warnings	Exact identifier application number: M020
BIOLUMIN-C HEAT AGING PROTECTOR SPF50	OCTOCRYLENE, HOMOSALATE, OCTISALATE, AND AVOBENZONE	Dermalogica, LLC.	38d0b78b-bd8e-4cb0-925a-19adff550c19	2024-10-16	Warnings	Exact identifier application number: M020
Vanicream Facial Moisturizer Broad Spectrum SPF30	ZINC OXIDE	Pharmaceutical Specialties Inc	d8c9a8d0-1f24-2240-e053-2a95a90a8dee	2024-10-15	Warnings	Exact identifier application number: M020
Mula Maldives SPF 30 Moisturizing Sunscreen	AVOBENZONE, OCTISALATE, OCTOCRYLENE	Mula Maldives PVT LTD	f9be092f-8d53-4bb2-8363-81c003da42d6	2024-10-15	Warnings	Exact identifier application number: M020
Kroger Invisible Sunscreen SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	THE KROGER COMPANY	f71ee1cd-e075-9ee9-e053-6394a90a8f9f	2024-10-15	Warnings	Exact identifier application number: M020
Kroger Sunscreen Oil SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	THE KROGER COMPANY	f76e12aa-9d98-5694-e053-6294a90a5256	2024-10-15	Warnings	Exact identifier application number: M020
Kroger Sport Sunscreen Broad Spectrum SPF 15	AVOBENZONE, HOMOSALATE, OCTISALATE	THE KROGER COMPANY	f0f350f4-b1b9-f4d3-e053-2995a90ac459	2024-10-15	Warnings	Exact identifier application number: M020
Kroger Shimmer Sunscreen Hydrating SPF 40	AVOBENZONE, OCTISALATE, OCTOCRYLENE	THE KROGER COMPANY	f76fe840-0da2-a903-e053-6294a90a05ee	2024-10-15	Warnings	Exact identifier application number: M020
MINERAL BASED SPF 50 SUNSCREEN	ZINC OXIDE, TITANIUM DIOXIDE	THE KROGER COMPANY	a4e6936d-a76c-e8fd-e053-2995a90a965f	2024-10-15	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