NDC11 00135081103
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 |
|---|---|
| 00135-0811-03 | 00135-0811 |
| 00135-0811-3 | 00135-0811 |
| 00135-811-03 | 00135-811 |
| 0135-0811-03 | 0135-0811 |
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 |
|---|---|---|---|---|---|---|
| Sensodyne Pronamel Clinical Enamel Strength Whitening Action | POTASSIUM NITRATE, SODIUM FLUORIDE | Haleon US Holdings LLC | e8a62f24-1db6-45fb-b6e1-5e57103f82bc | 2025-10-14 | Warnings | 0135-0811-03 0135-0811 00135081103 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.