NDC 68026-863 - La Prairie Concealer-Foundation Sunscreen SPF 15 WARM LINEN

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 68026-863
Package NDCs from labels: 68026-863-30
Manufacturer: La Prairie, Inc.
Effective date: 2025-02-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
La Prairie Concealer-Foundation Sunscreen SPF 15 - WARM LINEN	La Prairie, Inc.	2025-02-21	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
68026-863-30	La Prairie Concealer-Foundation Sunscreen SPF 15 WARM LINEN	30 mL in 1 BOTTLE	CREAM	30 mL	60 mg in 1mL	3
68026-863-30	La Prairie Concealer-Foundation Sunscreen SPF 15 WARM LINEN	1 in 1 BOX	CREAM		60 mg in 1mL	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
68026-863	LA PRAIRIE CONCEALER-FOUNDATION SUNSCREEN SPF 15 WARM LINEN (OCTINOXATE) KIT [LA PRAIRIE, INC.]	3	Unmatched	20250226_f2285eaa-39b4-86ae-e053-2a95a90ab7a0.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 195 of 195 · 3,889 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Essential Defense Everyday Clear Broad Spectrum SPF 47 Sunscreen	ZINC OXIDE AND OCTINOXATE	Allergan, Inc.	bc872876-20e7-40cb-b79d-68998883681a	2016-03-01	Warnings	Exact identifier unii: 4Y5P7MUD51
Antacid	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE AND SIMETHICONE	Safeway	d36b56a4-06f0-47ff-8add-4c327d60be22	2016-01-21	Warnings	Exact identifier unii: 5QB0T2IUN0 unii: 92RU3N3Y1O
Gas Relief	SIMETHICONE	Safeway	14a9fb00-707a-4b55-a060-82ad53a806e3	2016-01-08	Warnings	Exact identifier unii: 92RU3N3Y1O
TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted)	OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDE	Allergan, Inc.	6a996e03-907f-4e6a-b232-0892b86956b0	2015-08-21	Warnings	Exact identifier unii: 4Y5P7MUD51
Sodium Chloride	SODIUM CHLORIDE	Baxter Healthcare Corporation	2a96096d-43cc-49b7-af53-b53c17f41001	2014-07-25	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
SODIUM CHLORIDE	SODIUM CHLORIDE	Baxter Healthcare Corporation	b3b4b176-41f0-4ca8-90d4-3fba5707564a	2014-02-21		Exact identifier unii: 451W47IQ8X
TIS-U-SOL	SODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATE	Baxter Healthcare Corporation	9da4121f-d62d-4da4-8dfb-0494da16015f	2014-02-21		Exact identifier unii: 451W47IQ8X
Ringers	SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,	Baxter Healthcare Corporation	e1953d54-818d-46a6-8532-518ebae6d84e	2012-06-13		Exact identifier unii: 451W47IQ8X
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Baxter Healthcare Corporation	f09f80bf-2f8b-4420-865d-aec2d5e5cd4d	2012-06-12		Exact identifier unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.