NDC11 51316020728
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 |
|---|---|
| 51316-0207-28 | 51316-0207 |
| 51316-207-28 | 51316-207 |
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 |
|---|---|---|---|---|---|---|
| CVS Topical Analgesic Hemorrhoidal | DIBUCAINE | CVS PHARMACY,INC | b9e20531-3444-4955-b1d3-bb112340d230 | 2026-03-27 | Warnings | 51316-207-28 51316-207 51316020728 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.