NDC11 17089046721

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
17089-0467-21	17089-0467
17089-467-21	17089-467

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 DEFENSE	CALCIUM SULFIDE - CENTELLA ASIATICA - ECHINACEA ANGUSTIFOLIA WHOLE - ECHINACEA PURPUREA - THUJA OCCIDENTALIS LEAFY TWIG - VINCETOXICUM HIRUNDINARIA ROOT - PHYTOLACCA AMERICANA ROOT - SULFUR -	Guna spa	af94b281-be4f-4715-e053-2995a90af153	2021-12-15	Warnings	Exact identifier ndc (package): 17089-467-21 ndc (product): 17089-467 ndc11 (package): 17089046721

Reported adverse events (FAERS/openFDA)#

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