NDC11 51206031302
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 |
|---|---|
| 51206-0313-02 | 51206-0313 |
| 51206-0313-2 | 51206-0313 |
| 51206-313-02 | 51206-313 |
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 |
|---|---|---|---|---|---|---|
| Opal by Opalescence Complete | OPAL BY OPALESCENCE COMPLETE | Ultradent Products, Inc. | 249cc46a-dad6-0345-e063-6394a90a4447 | 2026-09-09 | Warnings | 51206-313-02 51206-313 51206031302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.