NDC11 80569008415

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
80569-0084-15	80569-0084
80569-084-15	80569-084

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
FLUSH Maximum Strength Antifungal formula	UNDECYLENIC ACID	Triple Point Group, LLC	1d9e56ef-c7c9-4aff-ab9e-b163e566e3d5	2023-11-11	Warnings	Exact identifier ndc (package): 80569-084-15 ndc (product): 80569-084 ndc11 (package): 80569008415

Reported adverse events (FAERS/openFDA)#

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