NDC11 73242112002

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
73242-1120-02	73242-1120
73242-1120-2	73242-1120

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
DENTI BUONGIORNO ORIGINAL TOOTH	SILICA, SODIUM MONOFLUOROPHOSPHATE	DONG IL PHARMS CO.,LTD	41197bb6-f6f4-c86d-e063-6294a90ad476	2025-10-14	Warnings	Exact identifier ndc (package): 73242-1120-2 ndc (product): 73242-1120 ndc11 (package): 73242112002

Reported adverse events (FAERS/openFDA)#

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