NDC11 57511000601

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
57511-0006-01	57511-0006
57511-0006-1	57511-0006
57511-006-01	57511-006

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
Allday 5000 Sensitive	1.1% SODIUM FLUORIDE TOOTHPASTE	Elevate Oral Care	401f5e96-095b-c001-e063-6394a90ab55e	2025-11-12	Warnings	Exact identifier ndc (package): 57511-0006-1 ndc (product): 57511-0006 ndc11 (package): 57511000601

Reported adverse events (FAERS/openFDA)#

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