NDC11 17312042214

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
17312-0422-14	17312-0422
17312-422-14	17312-422

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
Natural Eyes Complete Eye Relief Fast Dissolving Tables	EUPHRASIA OFFICIANALIS, HOITZIA, MERCURIUS CORROSIVUS, RUTA GRAVEOLENS, SULPHUR	TRP Company	30a1d9aa-3966-0b91-e063-6294a90ae72b	2025-03-18	Warnings	Exact identifier ndc (package): 17312-422-14 ndc (product): 17312-422 ndc11 (package): 17312042214

Reported adverse events (FAERS/openFDA)#

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