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 273 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Bali Body Cacao Tanning Oil SPF 15	OCTOCRYLENE, OCTISALATE, AVOBENZONE	Bali Body Pty Ltd	03c0b83d-0d85-9e69-e063-6394a90a6142	2024-10-21	Warnings	Exact identifier application number: M020
ALDI LACURA KIDS SPF 50 SUNSCREEN	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	ALDI INC	e34f37d7-02a5-0b72-e053-2a95a90acf83	2024-10-21	Warnings	Exact identifier application number: M020
Aldi Lacura Ultra Light Body SPF 100	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE	ALDI INC	f7ac082c-def8-4379-e053-6294a90a57e3	2024-10-21	Warnings	Exact identifier application number: M020
Aldi LACURA Sport Sunscreen 30 Broad Spectrum SPF 30 Continuous	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	ALDI INC	f7bdc1f7-d961-4596-e053-6394a90a1d87	2024-10-21	Warnings	Exact identifier application number: M020
Aldi LACURA Ultra Light Dry-Touch 100 Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE	ALDI INC	f7b2cf4e-468c-3406-e053-6394a90a2139	2024-10-21	Warnings	Exact identifier application number: M020
Aldi LACURA Sport Sunscreen 50 Broad Spectrum SPF 50 Continuous	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	ALDI INC	f7b32aa8-2e56-3725-e053-6294a90a18d2	2024-10-21	Warnings	Exact identifier application number: M020
Bliss Block Star Sheer Liquid Daily Sunscreen SPF 50 SPF-50	ZINC OXIDE	Bliss Products Holdings LLC	f262e5a7-3c57-a6d8-e053-2995a90aacbc	2024-10-21	Warnings	Exact identifier application number: M020
Berkley Jensen Sport Sunscreen SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	BJWC	fbd65277-7aff-de19-e053-6394a90a9496	2024-10-21	Warnings	Exact identifier application number: M020
Sun Bum SPF 15 Premium Moisturizing Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum, LLC	01bfe44c-655f-404c-981e-8d5f6728a738	2024-10-21	Warnings	Exact identifier application number: M020
Sun Bum SPF 70 Premium Moisturizing Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum, LLC	aa612570-b70a-4910-8086-6634834beb70	2024-10-21	Warnings	Exact identifier application number: M020
Premium Moisturizing Sunscreen SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum LLC	f5bd673a-46e5-43d5-9d76-8ddc5da70146	2024-10-21	Warnings	Exact identifier application number: M020
Sun Bum Kids Sunscreen SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Sun Bum LLC	6fcec9f9-bee0-4884-8c72-be273426f916	2024-10-21	Warnings	Exact identifier application number: M020
sunscreen	SKIN BARRIER SUN SHIELD SPF 30	True Botanicals, Inc.	d70eea23-7715-c17b-e053-2a95a90a839f	2024-10-18	Warnings	Exact identifier application number: M020
First Aid Only SunX30 Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Acme United Corporation	24c22903-8911-81d9-e063-6394a90a108b	2024-10-18	Warnings	Exact identifier application number: M020
TiZO Eye Renewal SPF 20 (Non-Tinted)	ZINC OXIDE	Fallien Cosmeceuticals, LTD	33f8760c-2953-44a6-9239-424fdb97a5b3	2024-10-18	Warnings	Exact identifier application number: M020
Fruit of the Earth Sun Town City SPF 30 Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Fruit of the Earth, Inc.	c85e5094-d442-55a9-e053-2995a90aed12	2024-10-18	Warnings	Exact identifier application number: M020
Bondi Sands SPF 60 Sunny Face	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	BONDI SANDS (USA) INC.	24c78897-3136-f24b-e063-6394a90aa80a	2024-10-18	Warnings	Exact identifier application number: M020
Fruit of the Earth Sun Town City Baby and Kids Mineral SPF 50 Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Fruit Of The Earth, Inc.	f42a0b1e-038d-4fab-e053-2995a90a5364	2024-10-18	Warnings	Exact identifier application number: M020
Cabana Beach Club with Manuka Honey and Essential Oils SPF 50 Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Fruit of the Earth, Inc.	f451c472-1d9f-1fbc-e053-2995a90a114e	2024-10-18	Warnings	Exact identifier application number: M020
Fruit of the Earth Sun Town City Mineral SPF 30 Sunscreen	ZINC OXIDE	Fruit Of The Earth, Inc.	f4490608-6cce-90f3-e053-2995a90a4930	2024-10-18	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