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		2026-10-23

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 151 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Activated Mineral Sunscreen Tinted	ACTIVATED MINERAL SUNSCREEN TINTED	Reve Skincare LLC	312a32a7-d253-f10c-e063-6294a90a803a	2025-12-04	Warnings	Exact identifier application number: M020
Everyday Humans Sunscreen Lip Balm Broad Spectrum SPF30	LIP BALM SPF30	Everyday Group Limted	2d42034a-4ada-57cf-e063-6394a90a0b5f	2025-12-04	Warnings	Exact identifier application number: M020
Ciele SPF 30 prime PROTECT Broad Spectrum SPF 30 Sunscreen	SUNSCREEN 30 MINERAL	LE COSMETICS INC	3bb54b93-0ab2-2ecc-e063-6394a90acac3	2025-12-04	Warnings	Exact identifier application number: M020
Good Times SPF 50 Sunscreen	HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE	EVERYDAY GROUP LIMITED	f40c6c4a-47a2-5dfe-e053-2995a90a3df3	2025-12-04	Warnings	Exact identifier application number: M020
Sheer Guard Natural Mineral Sunscreen	ZINC OXIDE	EVERYDAY GROUP LIMITED	3257719d-dcc6-7ac5-e063-6294a90aafcd	2025-12-04	Warnings	Exact identifier application number: M020
Sun Glazed SPF 30 Sunscreen Glow Oil	AVOBENZONE, HOMOSALATE, OCTOCRYLENE	EVERYDAY GROUP LIMITED	dba8075b-be36-4787-b23d-942d0e792aa8	2025-12-04	Warnings	Exact identifier application number: M020
Crunchi Sunlight Tinted Sunscreen SPF 30 Deep	ZINC OXIDE	Crunchi, LLC.	0dc478e0-9555-4ce6-b448-7d58e3a6bae0	2025-12-04	Warnings	Exact identifier application number: M020
Solbar Shield SPF40	SOLBAR SHIELD SPF40	Person and Covey	bd3a9a94-fc87-4127-abf9-29e56ac9ce5d	2025-12-04	Warnings	Exact identifier application number: M020
Solbar Thirty SPF 30	SOLBAR THIRTY SPF30	Person and Covey	ab9ac056-61d9-43d5-a3db-2d487897cc69	2025-12-04	Warnings	Exact identifier application number: M020
Solbar Fifty SPF50	SOLBAR FIFTY SPF50	Person and Covey	41fd3844-181c-4cb2-8379-f313104351ef	2025-12-04	Warnings	Exact identifier application number: M020
Solbar Avo SPF35	SOLBAR AVO SPF35	Person and Covey	bfe1e828-76d4-4db3-a8ba-b54b31baacad	2025-12-04	Warnings	Exact identifier application number: M020
Banana Boat Sport Ultra Broad Spectrum SPF 50 Plus Sunscreen Lip Balm	AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE	Edgewell Personal Care Brands LLC	c7a3c03b-7fee-404c-e053-2a95a90a3a97	2025-12-04	Warnings	Exact identifier application number: M020
Poolside Bronze Service Instant bronzing lotion. SPF30	HOMOSALATE,OCTOCRYLENE, OCTISALATE,OCTINOXATE, AVOBENZONE	Longway Technology(Guangzhou)Co.,Ltd.	4524129b-f8aa-171b-e063-6294a90aeebe	2025-12-04	Warnings	Exact identifier application number: M020
Solbar Zinc SPF38	SOLBAR ZINC SPF38	Person and Covey	fac62a2f-92ee-4afd-9999-bc5011159e43	2025-12-04	Warnings	Exact identifier application number: M020
elf Sun Boss Gloss SPF 25 Sunscreen Pink Me Girl	ZINC OXIDE	e.l.f. Cosmetics, Inc.	6c316ce4-c2f6-4633-a789-e786d0f76abd	2025-12-04	Warnings	Exact identifier application number: M020
Poolside Frostbite Sunscreen coconut SPF 15 Scented lip gloss	HOMOSALATE, OCTOCRYLENE, OCTISALATE , AVOBENZONE	Longway Technology(Guangzhou)Co.,Ltd.	452b5f2c-b61f-8915-e063-6294a90ac911	2025-12-04	Warnings	Exact identifier application number: M020
Poolside Frostbite Sunscreen watermelon SPF 15 Scented lip gloss	HOMOSALATE , OCTOCRYLENE, OCTISALATE, AVOBENZONE	Longway Technology(Guangzhou)Co.,Ltd.	452b6e12-1bf9-8093-e063-6394a90a9e74	2025-12-04	Warnings	Exact identifier application number: M020
Poolside Frostbite Sunscreen Papaya SPF 15 Scented lip gloss	HOMOSALATE,OCTOCRYLENE,OCTISALATE,AVOBENZONE	Longway Technology(Guangzhou)Co.,Ltd.	452b6f22-5080-86ab-e063-6394a90a0416	2025-12-04	Warnings	Exact identifier application number: M020
Poolside Golden Hour SPF15 sunscreen lip oil	HOMOSALATE,OCTOCRYLENE,OCTISALATE,AVOBENZONE	Longway Technology(Guangzhou)Co.,Ltd.	452b8393-1887-a660-e063-6394a90a4c2b	2025-12-04	Warnings	Exact identifier application number: M020
Poolside Sun Daze Body Illuminator SPF 30 shimmer sunscreen gel	HOMOSALATE,OCTOCRYLENE,OCTISALATE,AVOBENZONE	Longway Technology(Guangzhou)Co.,Ltd.	452b8dde-dd63-b585-e063-6394a90a3543	2025-12-04	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