NDC11 59088044605
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 |
|---|---|
| 59088-0446-05 | 59088-0446 |
| 59088-0446-5 | 59088-0446 |
| 59088-446-05 | 59088-446 |
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 | 59088-446-05 59088044605 |
| Atrix Acne Treatment | SALICYLIC ACID | PureTek Corporation | ba106b20-32aa-df90-e053-2995a90adaef | 2024-10-01 | Warnings | 59088-446-05 59088-446 59088044605 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.