NDC11 53125081729
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 |
|---|---|
| 53125-0817-29 | 53125-0817 |
| 53125-817-29 | 53125-817 |
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 |
|---|---|---|---|---|---|---|
| North Woods Derma Foam E-2 | BENZALKONIUM CHLORIDE | Superior Chemical Corporation | ab982dec-639a-277a-e053-2a95a90ac8b4 | 2024-11-18 | Warnings | 53125-817-29 53125-817 53125081729 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.