NDC11 59316020714

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
59316-0207-14	59316-0207
59316-207-14	59316-207

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Biofreeze Overnight Roll-on	MENTHOL	Reckitt Benckiser LLC	f67d7b7a-8922-73f6-e053-2995a90a2e80	2026-05-15	Warnings	Exact identifier ndc (package): 59316-207-14 ndc (product): 59316-207 ndc11 (package): 59316020714
Biofreeze Roll-On and Overnight Roll-On	MENTHOL	Reckitt Benckiser LLC	4d3dcb8f-2075-6bbc-e063-6394a90a4992	2026-05-15	Warnings	Exact identifier ndc (package): 59316-207-14 ndc11 (package): 59316020714