NDC11 17089006720

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
17089-0067-20	17089-0067
17089-067-20	17089-067

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
ANTI AGE STRESS	ACETYLCYSTEINE - BALLOTA FOETIDA - EPINEPHRINE - GLUTATHIONE - INTERFERON GAMMA-1B - LENOGRASTIM - LITHIUM CARBONATE - MELATONIN - PENICILLIUM GLABRUM - POTASSIUM CARBONATE - PUMMELO - RHODOTORULA RUBRA - SILVER NITRATE - STRYCHNOS NUX-VOMICA SEED - SUS SCROFA CEREBRAL CORTEX - SUS SCROFA STOMACH - SUS SCROFA SUPERIOR GASTRIC PLEXUS - SUS SCROFA THALAMUS -	Guna spa	ce25f3c5-20c9-4ba8-ac58-546febf142ec	2023-11-02	Warnings	Exact identifier ndc (package): 17089-067-20 ndc (product): 17089-067 ndc11 (package): 17089006720

Reported adverse events (FAERS/openFDA)#

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