NDC11 65278031901

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
65278-0319-01	65278-0319
65278-0319-1	65278-0319
65278-319-01	65278-319

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
Advanced Sun Resistance SPF 30	HOMOSALATE, OCTINOXATE, OXYBENZONE, OCTISALATE, AVOBENZONE	June Jacobs Labs, LLC	18f879f0-3d5b-0067-e063-6394a90a9db3	2024-05-21	Warnings	Exact identifier ndc (package): 65278-319-01 ndc (product): 65278-319 ndc11 (package): 65278031901

Reported adverse events (FAERS/openFDA)#

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