NDC11 54723000701
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 |
|---|---|
| 54723-0007-01 | 54723-0007 |
| 54723-0007-1 | 54723-0007 |
| 54723-007-01 | 54723-007 |
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 |
|---|---|---|---|---|---|---|
| Ombre Men overtime wipes | BENZOCAINE | Sambria Pharmaceuticals, LLC | 405f23ca-99c1-4db4-aba1-2fd7f93f55ee | 2025-10-07 | Warnings | 54723-007-01 54723-007 54723000701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.