NDC11 69517010904

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
69517-0109-04	69517-0109
69517-0109-4	69517-0109
69517-109-04	69517-109

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
All Day Pain Relief	NAPROXEN SODIUM TABLETS, 220 MG	HealthLife of USA LLC	7b0cb91e-5465-40ef-9f82-919f7d984f17	2017-06-01	Warnings	Exact identifier ndc (package): 69517-109-04 ndc (product): 69517-109 ndc11 (package): 69517010904

Reported adverse events (FAERS/openFDA)#

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