NDC11 68987000230
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 |
|---|---|
| 68987-0002-30 | 68987-0002 |
| 68987-002-30 | 68987-002 |
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 |
|---|---|---|---|---|---|---|
| PureLife Topical Anesthetic | BENZOCAINE | PureLife Dental | 9f2bdc10-6b41-4606-a65c-560d204fdb97 | 2025-01-08 | Warnings | 68987-002-30 68987-002 68987000230 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.