NDC11 70372072701
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 |
|---|---|
| 70372-0727-01 | 70372-0727 |
| 70372-0727-1 | 70372-0727 |
| 70372-727-01 | 70372-727 |
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 |
|---|---|---|---|---|---|---|
| BLT 1 | BENZOCAINE | CENTURA PHARMACEUTICALS INC | 3eea2171-850b-4045-e054-00144ff8d46c | 2026-01-15 | Warnings | 70372-727-01 70372-727 70372072701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.