NDC11 00924811000

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
00924-8110-0	00924-8110
00924-8110-00	00924-8110
0924-8110-00	0924-8110

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
First Aid Only Povidone-Iodine Prep Pad	POVIDONE-IODINE	Acme United Corporation	509b6c8e-6a9f-2656-e054-00144ff8d46c	2024-11-09	Warnings	Exact identifier ndc (package): 0924-8110-00 ndc (product): 0924-8110 ndc11 (package): 00924811000

Reported adverse events (FAERS/openFDA)#

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