NDC11 17089034618

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
17089-0346-18	17089-0346
17089-346-18	17089-346

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-PROSTATE	ALDESLEUKIN - BARIUM CARBONATE - CHASTE TREE - CHIMAPHILA UMBELLATA - CLEMATIS VITALBA - CONIUM MACULATUM FLOWERING TOP - DELPHINIUM STAPHISAGRIA SEED - DIGITALIS - FERRIC PICRATE - HUMAN INTERLEUKIN-10 (NONGLYCOSYLATED) - INTERFERON GAMMA-1B - MELATONIN - SAW PALMETTO - SELENIUM - SUS SCROFA PROSTATE - THUJA OCCIDENTALIS TWIG - TRANSFORMING GROWTH FACTOR BETA-1 - ZINC -	Guna spa	b99bb9ea-339c-4476-8e3c-e1fcbcfd5cda	2026-06-11	Warnings	Exact identifier ndc (package): 17089-346-18 ndc (product): 17089-346 ndc11 (package): 17089034618

Reported adverse events (FAERS/openFDA)#

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