NDC11 17089047621

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
17089-0476-21	17089-0476
17089-476-21	17089-476

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 HAY FEVER RELIEF	STRYCHNOS NUX VOMICA SEED - HISTAMINE DIHYDROCHLORIDE - MANGANESE - SCHOENOCAULON OFFICINALE SEED - APIS MELLIFERA - ARSENIC TRIOXIDE - SILVER NITRATE - ONION - EUPHRASIA STRICTA - GALPHIMIA GLAUCA FLOWERING TOP - SULFUR -	Guna spa	b8db4fc6-f235-6f2b-e053-2a95a90a186f	2021-12-15	Warnings	Exact identifier ndc (package): 17089-476-21 ndc (product): 17089-476 ndc11 (package): 17089047621

Reported adverse events (FAERS/openFDA)#

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