NDC11 84165001309

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
84165-0013-09	84165-0013
84165-0013-9	84165-0013
84165-013-09	84165-013

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 COLD HOT Pain Relief Gel Roll-On (Plantar Fasciitis)	MENTHOL	Guangzhou Zhupuyou E-commerce Co., Ltd	375bc794-3289-e610-e063-6294a90a4f9b	2025-06-12	Warnings	Exact identifier ndc (package): 84165-013-09 ndc (product): 84165-013 ndc11 (package): 84165001309