SkinCeuticals Physical Fusion UV Defense Broad Spectrum SPF 50 Sunscreen

Product NDC: 49967-077
11-digit product format: 499670077
Labeler code: 49967
Product ID: 49967-077_b9c31cda-e772-40f8-9d6b-9933ec4605ef
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: 2011-01-01
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: SkinCeuticals Physical Fusion UV Defense Broad Spectrum SPF 50 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
8df98d97-a5d2-4d52-8bd2-130a13501d60	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
49967-077-01	SkinCeuticals Physical Fusion UV Defense Broad Spectrum SPF 50 Sunscreen	1 in 1 CARTON	LOTION	1	12
49967-077-01	SkinCeuticals Physical Fusion UV Defense Broad Spectrum SPF 50 Sunscreen	50 mL in 1 BOTTLE	LOTION	50	12
49967-077-02	SkinCeuticals Physical Fusion UV Defense Broad Spectrum SPF 50 Sunscreen	4 mL in 1 TUBE	LOTION	4	12
49967-077-03	SkinCeuticals Physical Fusion UV Defense Broad Spectrum SPF 50 Sunscreen	125 mL in 1 BOTTLE	LOTION	125	12
49967-077-04	SkinCeuticals Physical Fusion UV Defense Broad Spectrum SPF 50 Sunscreen	250 mL in 1 BOTTLE	LOTION	250	12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
TITANIUM DIOXIDE	ACTIVE INGREDIENT	15FIX9V2JP	SKINCEUTICALS PHYSICAL FUSION UV DEFENSE BROAD SPECTRUM SPF 50 SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC]	4
ZINC OXIDE	ACTIVE INGREDIENT	SOI2LOH54Z	SKINCEUTICALS PHYSICAL FUSION UV DEFENSE BROAD SPECTRUM SPF 50 SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC]	4
TITANIUM DIOXIDE	ACTIVE MOIETY	15FIX9V2JP	SKINCEUTICALS PHYSICAL FUSION UV DEFENSE BROAD SPECTRUM SPF 50 SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC]	4
ZINC OXIDE	ACTIVE MOIETY	SOI2LOH54Z	SKINCEUTICALS PHYSICAL FUSION UV DEFENSE BROAD SPECTRUM SPF 50 SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC]	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49967-077	SKINCEUTICALS PHYSICAL FUSION UV DEFENSE BROAD SPECTRUM SPF 50 SUNSCREEN (TITANIUM DIOXIDE AND ZINC OXIDE) LOTION [L'OREAL USA PRODUCTS INC]	12	Current NDC, Legacy NDC, 5 package rows	20240717_8df98d97-a5d2-4d52-8bd2-130a13501d60.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 114 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Kind Restore Tinted Mineral Sunscreen	ZINC OXIDE	POLISH BEAUTY	3980d278-c0f4-2c59-e063-6394a90aac37	2025-12-16		Exact identifier application number: M020
Solar Eclipse Extreme Sunscreen	ZINC OXIDE	ULTRAVIOLET SKINCARE LLC	36bfa691-48c0-8033-e063-6294a90ad899	2025-12-16		Exact identifier application number: M020
Kind Restore Moisturizing Lip Balm	TITANIUM DIOXIDE, ZINC OXIDE	POLISH BEAUTY	39814e27-4f3f-5ee6-e063-6394a90a941b	2025-12-16		Exact identifier application number: M020
Yoali SPF 40	ZINC OXIDE	YOALI STUDIO LLC	390b7f9c-bc04-80ec-e063-6294a90a4092	2025-12-16		Exact identifier application number: M020
Skin Defense Matte Tinted Sunscreen	ZINC OXIDE	Gentlehomme LLC	365eb727-3e7f-f1dd-e063-6394a90aa469	2025-12-16		Exact identifier application number: M020
Dr B Clinical Skin Care Tinted Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	NAIRA BABAIAN, M.D., P.A.	365da1f8-5250-7589-e063-6294a90a3e68	2025-12-16		Exact identifier application number: M020
Dr B Clinical Skin Care Non Tinted Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	NAIRA BABAIAN, M.D., P.A.	365d7564-3025-257b-e063-6294a90ad170	2025-12-16		Exact identifier application number: M020
Tinted Mineral Sunscreen	ZINC OXIDE	Gentlehomme LLC	365e7d8e-e3e0-4c08-e063-6294a90af415	2025-12-16		Exact identifier application number: M020
Daily Replenish mineral sunscreen	ZINC OXIDE	PURE VITALITY SKIN AND BODY, INC	369896b1-f4b4-6201-e063-6394a90a5bca	2025-12-16		Exact identifier application number: M020
Zinc 20 mineral sunscreen face Plus body	ZINC OXIDE	PURE VITALITY SKIN AND BODY, INC	36985373-22dd-2232-e063-6394a90a76fb	2025-12-16		Exact identifier application number: M020
Matte Defense Mineral Sunscreen non tinted	TITANIUM DIOXIDE, ZINC OXIDE	PURE VITALITY SKIN AND BODY, INC	3698090a-1639-00f9-e063-6394a90a7dd1	2025-12-16		Exact identifier application number: M020
Daily Replenish mineral sunscreen	ZINC OXIDE	PURE VITALITY SKIN AND BODY, INC	3698d309-b9bf-e197-e063-6294a90af5a1	2025-12-16		Exact identifier application number: M020
Zinc 20 mineral sunscreen face Plus body	ZINC OXIDE	PURE VITALITY SKIN AND BODY, INC	3698f29e-5d80-94af-e063-6394a90a0489	2025-12-16		Exact identifier application number: M020
Tinted Mineral Primer SPF 40	TITANIUM DIOXIDE, ZINC OXIDE	JOSEPHINA RAMIREZ	365cf2be-8862-3622-e063-6394a90ac4e3	2025-12-16		Exact identifier application number: M020
SANCTUARY Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	CHAMPAGNE APOTHECARY LLC	365ca99c-c878-1f4b-e063-6394a90a1f53	2025-12-16		Exact identifier application number: M020
Tinted Mineral Defense SPF 40	ZINC OXIDE	JOSEPHINA RAMIREZ	365d299a-5886-5597-e063-6394a90a336c	2025-12-16		Exact identifier application number: M020
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	MILL VALLEY DERMATOLOGY, INC.	3b171a89-c757-47a1-e063-6294a90a7a64	2025-12-16	Warnings	Exact identifier application number: M020
Tinted BB Cream	ZINC OXIDE	Eco Esthetics LLC	38f3e618-59e1-4504-e063-6394a90afa55	2025-12-16		Exact identifier application number: M020
Tinted Mineral Sunscreen	ZINC OXIDE	MADRE TIERRA, INC.	3f697463-d3db-7b73-e063-6394a90ac222	2025-12-16	Warnings	Exact identifier application number: M020
Non-Tinted Replenishing Daily Protection	ZINC OXIDE	MADRE TIERRA, INC.	3f69d6f3-454b-e60a-e063-6394a90a8781	2025-12-16	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
49967-077-01	49967007701	1 BOTTLE in 1 CARTON (49967-077-01) / 50 mL in 1 BOTTLE	1 bottle	2011-01-01	0000-00-00	No	No	Current
49967-077-02	49967007702	4 mL in 1 TUBE (49967-077-02)	4 ml	2011-01-01	0000-00-00	No	No	Current
49967-077-03	49967007703	125 mL in 1 BOTTLE (49967-077-03)	125 ml	2011-01-01	0000-00-00	No	No	Current
49967-077-04	49967007704	250 mL in 1 BOTTLE (49967-077-04)	250 ml	2011-01-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts	L'Oreal USA Products Inc \| Goodier Cosmetics LP \| Beauty Manufacturing Solutions Corp.	2024-07-16	HUMAN OTC DRUG LABEL	12