NDC11 79903027910

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
79903-0279-10	79903-0279
79903-279-10	79903-279

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
Alcohol-Free Anticavity	SODIUM FLUORIDE	Walmart Inc.	1fd2f3ca-066e-282a-e063-6294a90a05a9	2026-02-27	Warnings, Adverse reactions	Exact identifier ndc (package): 79903-279-10 ndc (product): 79903-279 ndc11 (package): 79903027910

Reported adverse events (FAERS/openFDA)#

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