NDC11 51316021701

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
51316-0217-01	51316-0217
51316-0217-1	51316-0217
51316-217-01	51316-217

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
CVS SPF 50 Face Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	CVS	26a69a47-947a-a478-e063-6394a90aa468	2025-09-16	Warnings	Exact identifier ndc (package): 51316-217-01 ndc (product): 51316-217 ndc11 (package): 51316021701

Reported adverse events (FAERS/openFDA)#

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