NDC11 21749011440

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
21749-0114-40	21749-0114
21749-114-40	21749-114

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 Antimicrobial Fragrance Free Foaming Hand SP	BENZALKONIUM CHLORIDE	GOJO Industries, Inc.	4477d823-3658-43ac-bb51-fd20888606c9	2024-12-31	Warnings	Exact identifier ndc (package): 21749-114-40 ndc (product): 21749-114 ndc11 (package): 21749011440

Reported adverse events (FAERS/openFDA)#

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