NDC11 66975070002

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
66975-0700-02	66975-0700
66975-0700-2	66975-0700
66975-700-02	66975-700

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
PRO-SYS	SODIUM FLUORIDE AND POTASSIUM NITRATE	Benco Dental	4e470ba4-60bb-1815-e063-6294a90abacc	2025-12-01	Warnings	Exact identifier ndc (package): 66975-700-02 ndc (product): 66975-700 ndc11 (package): 66975070002

Reported adverse events (FAERS/openFDA)#

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