NDC11 69367031801

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
69367-0318-01	69367-0318
69367-0318-1	69367-0318
69367-318-01	69367-318

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 and Potassium Nitrate	SODIUM FLUORIDE AND POTASSIUM NITRATE	Westminster Pharmaceuticals, LLC	7a051d80-879d-4995-96ef-77b60dad26b7	2024-04-18	Warnings, Adverse reactions	Exact identifier ndc (package): 69367-318-01 ndc (product): 69367-318 ndc11 (package): 69367031801

Reported adverse events (FAERS/openFDA)#

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