NDC11 52000006002
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 |
|---|---|
| 52000-0060-02 | 52000-0060 |
| 52000-0060-2 | 52000-0060 |
| 52000-060-02 | 52000-060 |
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 |
|---|---|---|---|---|---|---|
| Oral Pain Relief | BENZOCAINE AND BENZALKONIUM CHLORIDE | Universal Distribution Center LLC | 18520f9b-4d35-1e9c-e063-6294a90aaa39 | 2025-10-30 | Warnings | 52000-060-02 52000-060 52000006002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.