NDC11 53208056800
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 |
|---|---|
| 53208-0568-0 | 53208-0568 |
| 53208-0568-00 | 53208-0568 |
| 53208-568-00 | 53208-568 |
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 |
|---|---|---|---|---|---|---|
| EUTHYMOL WHITENING SET | SODIUM FLUORIDE | LG HOUSEHOLD & HEALTH CARE LTD. | 35839b10-4c40-40e5-e063-6294a90a85b4 | 2025-05-19 | Warnings | 53208-568-00 53208-568 53208056800 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.