NDC11 21749080289

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
21749-0802-89	21749-0802
21749-802-89	21749-802

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
PURELL Advanced E3 Rated Instant Hand Sanitizer Foam	ALCOHOL	GOJO Industries, Inc.	1f78370b-132a-4759-8cbc-b5e093f90f8d	2024-12-12	Warnings	Exact identifier ndc (package): 21749-802-89 ndc (product): 21749-802 ndc11 (package): 21749080289

Reported adverse events (FAERS/openFDA)#

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