NDC11 00135403201

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
00135-4032-01	00135-4032
00135-4032-1	00135-4032
0135-4032-01	0135-4032

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
Sensodyne Cavity and Sensitivity	POTASSIUM NITRATE, SODIUM FLUORIDE	Haleon US Holdings LLC	d002074b-0580-4247-b3c7-121b8c098697	2025-11-24	Warnings	Exact identifier ndc (package): 0135-4032-01 ndc (product): 0135-4032 ndc11 (package): 00135403201

Reported adverse events (FAERS/openFDA)#

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