NDC11 17089030220

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
17089-0302-20	17089-0302
17089-302-20	17089-302

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-STOMACH	ACTIVATED CHARCOAL - ANTIMONY TRISULFIDE - BISMUTH SUBNITRATE - DIOSCOREA VILLOSA ROOT - DOPAMINE - HUMAN EPIDERMAL GROWTH FACTOR - IPECAC - OREGANO - PICEA MARIANA RESIN - ROBINIA PSEUDOACACIA BARK - SEMECARPUS ANACARDIUM JUICE - SILVER NITRATE - SUS SCROFA STOMACH - SUS SCROFA SYMPATHETIC NERVE - MOMORDICA BALSAMINA IMMATURE FRUIT -	Guna spa	7805055c-e5f6-4d1d-9449-a5dce8a066eb	2022-11-15	Warnings	Exact identifier ndc (package): 17089-302-20 ndc (product): 17089-302 ndc11 (package): 17089030220

Reported adverse events (FAERS/openFDA)#

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