NDC11 59316000503

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
59316-0005-03	59316-0005
59316-0005-3	59316-0005
59316-005-03	59316-005

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 Relief	MENTHOL, UNSPECIFIED FORM	Reckitt Benckiser LLC	07be6e88-1850-4d6a-946d-f03830b8c4a2	2026-05-15	Warnings	Exact identifier ndc (package): 59316-005-03 ndc (product): 59316-005 ndc11 (package): 59316000503
Biofreeze Day and Overnight	MENTHOL	Reckitt Benckiser LLC	fb5c8f89-a720-ad32-e053-6294a90a2abe	2026-05-13	Warnings	Exact identifier ndc (package): 59316-005-03 ndc11 (package): 59316000503

Reported adverse events (FAERS/openFDA)#

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