NDC11 17089030118

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
17089-0301-18	17089-0301
17089-301-18	17089-301

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-DIGEST	ANGELICA ARCHANGELICA ROOT - ANISUM - ARTEMISIA ABROTANUM FLOWERING TOP - ASCORBIC ACID - CITRULLUS COLOCYNTHIS FRUIT PULP - GENTIANA LUTEA ROOT - MELATONIN - NIACIN - PANCRELIPASE AMYLASE - PANCRELIPASE LIPASE - PORK LIVER - SEROTONIN - STRYCHNOS NUX-VOMICA SEED - SUS SCROFA DIENCEPHALON - SUS SCROFA DUODENUM - SUS SCROFA GALL BLADDER - SUS SCROFA PANCREAS - SUS SCROFA PYLORUS - THIAMINE HYDROCHLORIDE - TRYPSIN - TRYPTOPHAN -	Guna spa	624228b9-70be-43a1-93a5-f6e708814fa2	2018-12-22	Warnings	Exact identifier ndc (package): 17089-301-18 ndc (product): 17089-301 ndc11 (package): 17089030118

Reported adverse events (FAERS/openFDA)#

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