NDC11 72937063203

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
72937-0632-03	72937-0632
72937-0632-3	72937-0632
72937-632-03	72937-632

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
MENTHOL	MENTHOL	SUNSET PAIN RELIEF	45c5ca6f-d425-6cfb-e063-6394a90a1b66	2025-12-20	Warnings	Exact identifier ndc (package): 72937-632-03 ndc (product): 72937-632 ndc11 (package): 72937063203

Reported adverse events (FAERS/openFDA)#

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