NDC11 17089041518
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 |
|---|---|
| 17089-0415-18 | 17089-0415 |
| 17089-415-18 | 17089-415 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| EUBIOFLOR | ACTIVATED CHARCOAL - AETHUSA CYNAPIUM - ALTHAEA OFFICINALIS LEAF - BILBERRY - CANDIDA ALBICANS - UNCARIA TOMENTOSA - ESCHERICHIA COLI - INDOLE - MERCURIUS SOLUBILIS - OKOUBAKA AUBREVILLEI BARK - PORK LIVER - PROTEUS VULGARIS - SILYBUM MARIANUM SEED - SKATOLE - STRYCHNOS NUX-VOMICA SEED - SUS SCROFA COLON - SUS SCROFA GALL BLADDER - SUS SCROFA PANCREAS - TABEBUIA IMPETIGINOSA BARK - TARAXACUM OFFICINALE - VERATRUM ALBUM ROOT - | Guna spa | 7dacc28a-2185-4566-8e83-c7a70338797f | 2026-06-10 | Warnings | 17089-415-18 17089-415 17089041518 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.