NDC11 59088071300
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 |
|---|---|
| 59088-0713-0 | 59088-0713 |
| 59088-0713-00 | 59088-0713 |
| 59088-713-00 | 59088-713 |
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 |
|---|---|---|---|---|---|---|
| Atrix System 1 | SALICYLIC ACID | PureTek Corporation | c8d50ce6-5580-d3ef-e053-2a95a90a01d2 | 2024-12-13 | Warnings | 59088-713-00 59088-713 59088071300 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.