NDC11 17089046218

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
17089-0462-18	17089-0462
17089-462-18	17089-462

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 LYMPHO DETOX	AESCULUS HIPPOCASTANUM - APIS MELLIFERA - CALENDULA OFFICINALIS FLOWER - HEXAKETOCYCLOHEXANE - EQUISETUM HYEMALE - FUMARIC ACID - GRAPHITE - HYDRASTIS CANADENSIS - HYDROCOTYLE ASIATICA - JUGLANS REGIA - LEVOTHYROXINE - MAGNESIUM PHOSPHATE - MALIC ACID - MYOSOTIS ARVENSIS - PHYTOLACCA AMERICANA ROOT - SARSAPARILLA - SODIUM DIETHYL OXALACETATE - SODIUM PYRUVATE - SUS SCROFA PLACENTA - TARAXACUM OFFICINALE -	Guna spa	aeb71e21-2fdb-6b84-e053-2995a90a4c01	2020-10-23	Warnings	Exact identifier ndc (package): 17089-462-18 ndc (product): 17089-462 ndc11 (package): 17089046218

Reported adverse events (FAERS/openFDA)#

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