NDC11 80070022033
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 |
|---|---|
| 80070-0220-33 | 80070-0220 |
| 80070-220-33 | 80070-220 |
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 |
|---|---|---|---|---|---|---|
| Anbesol Maximum Strength | BENZOCAINE | Foundation Consumer Brands | dcc37403-0192-4658-bb7a-059273ce0047 | 2026-06-22 | Warnings | 80070-220-33 80070-220 80070022033 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.