NDC11 17089050118

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
17089-0501-18	17089-0501
17089-501-18	17089-501

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 FEMALE SUPPORT	LILIUM LANCIFOLIUM WHOLE FLOWERING - SUS SCROFA OVARY - SUS SCROFA PITUITARY GLAND - SEPIA OFFICINALIS JUICE - ADENOSINE CYCLIC PHOSPHATE - PULSATILLA VULGARIS - SUS SCROFA HYPOTHALAMUS - SUS SCROFA ADRENAL GLAND - SUS SCROFA PANCREAS - MAGNESIUM PHOSPHATE DIBASIC TRIHYDRATE	Guna spa	bb22182f-a503-433f-e053-2995a90a2f47	2021-02-12	Warnings	Exact identifier ndc (package): 17089-501-18 ndc (product): 17089-501 ndc11 (package): 17089050118

Reported adverse events (FAERS/openFDA)#

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