NDC11 17089034718

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
17089-0347-18	17089-0347
17089-347-18	17089-347

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
GUNA-HYPERTENSION	ARNICA MONTANA - FUMARIC ACID - GOLD - LEAD - MELATONIN - MELILOTUS - OLEA EUROPAEA FLOWER - PORK KIDNEY - RAUWOLFIA SERPENTINA - SODIUM PYRUVATE - SPIGELIA - SUS SCROFA ADRENAL GLAND - SUS SCROFA DIENCEPHALON - UBIDECARENONE - VISCUM ALBUM FRUIT -	Guna spa	40c5b156-dc5c-41c2-88c3-a9bf28119d22	2018-12-21	Warnings	Exact identifier ndc (package): 17089-347-18 ndc (product): 17089-347 ndc11 (package): 17089034718

Reported adverse events (FAERS/openFDA)#

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