NDC11 50268073356

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
50268-0733-56	50268-0733
50268-733-56	50268-733

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
Sodium Fluoride Gel	SODIUM FLUORIDE	AvPAK	de973f9c-af34-4977-e053-2995a90a54a0	2026-01-09	Warnings, Adverse reactions	Exact identifier ndc (package): 50268-733-56 ndc (product): 50268-733 ndc11 (package): 50268073356

Reported adverse events (FAERS/openFDA)#

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