NDC11 62742425501

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
62742-4255-01	62742-4255
62742-4255-1	62742-4255

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Daily Prevention Ultra Defense Moisturizer SPF 50	HOMOSALATE, OCTISALATE,OCTOCRYLENE AND ZINC OXIDE	Allure Labs	14070076-8c57-e2f1-e063-6394a90a0dfc	2024-03-19	Warnings	Exact identifier ndc (package): 62742-4255-1 ndc (product): 62742-4255 ndc11 (package): 62742425501

Reported adverse events (FAERS/openFDA)#

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