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 269 of 346 · 6,912 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Banana Boat	ZINC OXIDE	Edgewell Personal Care Brands LLC	1ce728be-966e-b662-e063-6394a90a0ba8	2024-10-30	Warnings	Exact identifier application number: M020
RECIPE Infinite UV Shield Sunscreen Broad Spectrum SPF100	AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE	COSMAX USA, INC.	2596a17e-4042-3544-e063-6294a90aa4c9	2024-10-29	Warnings	Exact identifier application number: M020
Sunblocz	ZINC OXIDE	Olen Skin Care Corporation	36fec1f1-5e8b-5764-e054-00144ff8d46c	2024-10-29	Warnings	Exact identifier application number: M020
Sunblocz Baby and Kids	ZINC OXIDE	Olen Skin Care Corporation	35cbb9d5-639c-207a-e054-00144ff88e88	2024-10-29	Warnings	Exact identifier application number: M020
ZO Skin Health Daily Sheer Broad-Spectrum Sunscreen SPF 50 Water Resistant (40 Minutes)	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	ZO Skin Health, Inc.	fd7d40fe-178a-e1b1-e053-6294a90a29a1	2024-10-29	Warnings	Exact identifier application number: M020
ZO Skin Health Sunscreen Plus Primer Broad-Spectrum SPF 30	TITANIUM DIOXIDE AND ZINC OXIDE	ZO Skin Health, Inc.	9a4f5be1-da04-48b9-897a-57f4a3d9d1ec	2024-10-29	Warnings	Exact identifier application number: M020
TiZO Ultra Zinc SPF 40 (Non-Tinted)	ZINC OXIDE	Fallien Cosmeceuticals, LTD	e4a06973-21bb-4eda-9b74-fc23bee141ab	2024-10-29	Warnings	Exact identifier application number: M020
TiZO Ultra Zinc SPF 40 (Tinted)	ZINC OXIDE	Fallien Cosmeceuticals, LTD	36efd48b-910e-4b61-9519-a6d5c7e9a7c3	2024-10-29	Warnings	Exact identifier application number: M020
ZO Skin Health Broad-Spectrum Sunscreen SPF 50	TITANIUM DIOXIDE, ZINC OXIDE	ZO Skin Health, Inc.	d817f80b-a998-b67e-e053-2995a90a1971	2024-10-29	Warnings	Exact identifier application number: M020
SPF 15 Coconut Lip Balm	ZINC OXIDE	Naples Soap Company, Inc.	25a7510f-5ef3-9920-e063-6394a90a2079	2024-10-29	Warnings	Exact identifier application number: M020
Defense Total High Protection SPF 50 No Color Daily Non-Greasy Face Protection	HOMOSALATE, OCTOCRYLENE, AVOBENZONE	Bel Star S.A. (Colombia)	a7d69691-cecc-798e-e053-2a95a90a995f	2024-10-28	Warnings	Exact identifier application number: M020
LBEL FOREVER ULTRA MATTE BASE CONTROL BRILLO DE LARGA DURACION FPS 15 SHINE CONTROL LONGWEAR FOUNDATION SPF 15 LATTE 180-F	OCTINOXATE, ZINC OXIDE	Bel Star S.A.	eea17271-e8c8-ab21-e053-2995a90a2fcc	2024-10-28	Warnings	Exact identifier application number: M020
LBEL SPECIALISTE DARK SPOT BRIGHTENING MOISTURIZING SPF 30	AVOBENZONE, OCTISALATE, OCTOCRYLENE	BEL STAR SA	fd90ffc6-a1e1-e02e-e053-6294a90a4e7c	2024-10-28	Warnings	Exact identifier application number: M020
LBEL SOLUTIONS PRO-HIALURON BASE SERUM CON EFECTO RELLENO DE ARRUGAS FPS 15 WRINKLE FILLER EFFECT SERUM FOUNDATION SPF 15 CHAMPAGNE 170-N	OCTINOXATE, ZINC OXIDE	BEL STAR S.A.	0b782198-58e7-5343-e063-6294a90a3713	2024-10-28	Warnings	Exact identifier application number: M020
FHF Elevated Shade 100% Mineral Sunscreen	SUNSCREEN	Owen Biosciences Inc	dabd3b95-01d3-014c-e053-2a95a90a0fec	2024-10-28	Warnings	Exact identifier application number: M020
RECIPE Infinite UV Shield Sunscreen Broad Spectrum SPF100	AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE	BAY BELLE LABS	259653e7-dfe0-44a2-e063-6294a90a416d	2024-10-28	Warnings	Exact identifier application number: M020
Banana Boat	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Edgewell Personal Care Brands LLC	8a21acbe-2f3d-cf78-e053-2a95a90a77f6	2024-10-27	Warnings	Exact identifier application number: M020
Banana Boat	AVOBENZONE, HOMOSALATE, OCTOCRYLENE	Edgewell Personal Care Brands LLC	7961ff9f-75db-4977-e053-2a91aa0ae628	2024-10-27	Warnings	Exact identifier application number: M020
Banana Boat Light as air face SUNSCREEN UVA UVB Broad Spectrum SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Edgewell Personal Care Brands LLC	8a1c9a3c-394e-9122-e053-2995a90acb23	2024-10-27	Warnings	Exact identifier application number: M020
Banana Boat	AVOBENZONE, HOMOSALATE, OCTOCRYLENE	Edgewell Personal Care Brands LLC	8b889b75-07ac-4276-e053-2a95a90a69c6	2024-10-27	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