NDC11 87203000103
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 |
|---|---|
| 87203-0001-03 | 87203-0001 |
| 87203-0001-3 | 87203-0001 |
| 87203-001-03 | 87203-001 |
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 |
|---|---|---|---|---|---|---|
| 5 Elementum Delay Wipes | BENZOCAINE DELAY WIPES | MSVenturesGroup O | 440539b0-612b-3b41-e063-6294a90a1ddd | 2026-02-05 | Warnings | 87203-001-03 87203-001 87203000103 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.