NDC11 17089023520

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
17089-0235-20	17089-0235
17089-235-20	17089-235

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-TONSILS	ANGELICA SINENSIS ROOT - BINETRAKIN - INTERLEUKIN-3 - LENOGRASTIM - MELATONIN - REISHI - SHIITAKE MUSHROOM - SUS SCROFA BLOOD - SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE - SUS SCROFA SPLEEN - INTERLEUKIN-11 -	Guna spa	b7d0a24f-c702-4b4a-8494-a4cbbb020257	2018-12-21	Warnings	Exact identifier ndc (package): 17089-235-20 ndc (product): 17089-235 ndc11 (package): 17089023520

Reported adverse events (FAERS/openFDA)#

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