La Roche Posay Laboratoire Dermatologique

Product NDC: 49967-907
Requested package NDC: 49967-907-01
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

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 100 of 353 · 7,041 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ageless Glow Serum BB Cream Sunscreen SPF 40 - Medium Tan	HOMOSALATE, TITANIUM DIOXIDE, ZINC OXIDE	Pur-lisse Beauty, LLC	47387d5f-e77b-5633-e063-6294a90a5584	2025-12-30	Warnings	Exact identifier application number: M020
Ageless Glow Serum BB Cream Sunscreen SPF 40 - Tan	HOMOSALATE, TITANIUM DIOXIDE, ZINC OXIDE	Pur-lisse Beauty, LLC	4738be66-0fe8-148e-e063-6394a90a1b02	2025-12-30	Warnings	Exact identifier application number: M020
Ageless Glow Serum BB Cream Sunscreen SPF 40 - Tan Deep	HOMOSALATE, TITANIUM DIOXIDE, ZINC OXIDE	Pur-lisse Beauty, LLC	4738eed1-9f72-5fd8-e063-6394a90a26bd	2025-12-30	Warnings	Exact identifier application number: M020
Ageless Glow Serum BB Cream Sunscreen SPF 40 - Deep	HOMOSALATE, TITANIUM DIOXIDE, ZINC OXIDE	Pur-lisse Beauty, LLC	4739179e-88b3-8820-e063-6394a90aa211	2025-12-30	Warnings	Exact identifier application number: M020
WHITE TEA TINTED MOISTURIZER	WHITE TEA TINTED MOISTURIZER BROAD SPECTRUM SPF 30 SUNSCREEN	GLOW CONCEPT INC	eb2df93f-6cdc-7ae8-e053-2a95a90a0091	2025-12-29	Warnings	Exact identifier application number: M020
Hawaiian Natural Zinc Sunscreen SPF 50	ZINC OXIDE	Kokua Sun Care	64a5589b-735d-38ba-e053-2a91aa0ad8f4	2025-12-29	Warnings	Exact identifier application number: M020
Hawaiian Natural Zinc Sunscreen Broad Spectrum Tinted SPF 30	ZINC OXIDE	Kokua Sun Care	f9a12dac-2fd0-798f-e053-6394a90aa784	2025-12-29	Warnings	Exact identifier application number: M020
Calming Days Vegan Sunscreen	,OCTYL TRIAZONE (ETHYLHEXYL TRIAZONE), BISOCTRIZOLE, DIETHYLHEXYL BUTAMIDO TRIAZONE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE	MERCYCO Co., Ltd.	38898014-eefe-73ec-e063-6394a90a3738	2025-12-29	Warnings	Exact identifier application number: M020
SPF 30 Sunscreen	ZINC OXIDE, TITANIUM DIOXIDE	CLEURE	f5512f34-08ee-b0f6-e053-2a95a90ab5bd	2025-12-29	Warnings	Exact identifier application number: M020
COCO AND EVE SUNNY HONEY PROTECT TAN BOOSTING ANTI-AGING SPF 20	SUNSCREEN OIL	Soleil Collective LLC	471b3028-2c13-ab70-e063-6394a90aa660	2025-12-29	Warnings	Exact identifier application number: M020
COCO AND EVE SUNNY HONEY PROTECT TAN BOOSTING ANTI-AGING SPF 45	SUNSCREEN OIL	Soleil Collective LLC	471c0eed-f7ca-3c3b-e063-6294a90ad2c6	2025-12-29	Warnings	Exact identifier application number: M020
EIGHT HOUR NOURISHING LIP SPF 20	OCTINOXATE, AVOBENZONE	REVLON	b3c16e60-752d-6eba-e053-2995a90a2b20	2025-12-29	Warnings	Exact identifier application number: M020
CERAMIDE PREMIERE BROAD SPECTRUM SPF 30	OCTINOXATE, OCTISALATE, OXYBENZONE, OCTOCRYLENE, AVOBENZONE	REVLON	b3358bfd-7fe5-33e2-e053-2a95a90ac2ea	2025-12-29	Warnings	Exact identifier application number: M020
Prevage anti aging SPF 30	OCTISALATE, OCTINOXATE, OXYBENZONE, AVOBENZONE, OCTOCRYLENE,	Revlon	b2bff796-1579-2686-e053-2995a90ad6c7	2025-12-29	Warnings	Exact identifier application number: M020
FLAWLESS FUTURE SPF 30	OCTINOXATE, OCTISALATE, OXYBENZONE, AVAOBENZONE	REVLON	b553aec1-5002-3a3f-e053-2995a90a22e5	2025-12-29	Warnings	Exact identifier application number: M020
Prevage Anti-aging eye cream SPF 15	OCTINOXATE, OXYBENZONE	Revlon	b2a92d72-e634-7379-e053-2995a90a2bca	2025-12-29	Warnings	Exact identifier application number: M020
Prevage Anti-aging Moisture Cream	OCTINOXATE, OCTISALATE, OXYBENZONE, OCTOCRYLENE, AVOBENZONE	Revlon Consumer Products Corp	b247adbe-dfe8-df0a-e053-2995a90a34d9	2025-12-29	Warnings	Exact identifier application number: M020
Sheer Protection SPF 30	ZINC OXIDE	Skin Script, LLC	0450dcc9-3f8f-e2c2-e063-6294a90af60b	2025-12-29	Warnings	Exact identifier application number: M020
RE-NUTRIV ULTRA RADIANCE MAKEUP BROAD SPECTRUM SPF 20	OCTINOXATE AND TITANIUM DIOXIDE	ESTEE LAUDER INC	897b8edb-f089-4a49-baca-e05806b0a068	2025-12-29	Warnings	Exact identifier application number: M020
Mine Line Coconut Sunscreen SPF 50	ZINC OXIDE	Spa de Soleil	4642b1cc-43b1-6997-e063-6394a90ac764	2025-12-29	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	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

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