NDC11 51452003706

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
51452-0037-06	51452-0037
51452-0037-6	51452-0037
51452-037-06	51452-037

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
Point Relief cold Spot Pain Relieving roll-on	MENTHOL	Fabrication Enterprises	3f1db0ad-aaa8-4e14-9349-45057e0fb4a6	2023-11-05	Warnings	Exact identifier ndc (package): 51452-037-06 ndc (product): 51452-037 ndc11 (package): 51452003706

Reported adverse events (FAERS/openFDA)#

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