NDC11 00135060102
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 |
|---|---|
| 00135-0601-02 | 00135-0601 |
| 00135-0601-2 | 00135-0601 |
| 00135-601-02 | 00135-601 |
| 0135-0601-02 | 0135-0601 |
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 |
|---|---|---|---|---|---|---|
| parodontax | STANNOUS FLUORIDE | Haleon US Holdings LLC | 0f07aa1a-97be-44af-92d8-a10777e24e0a | 2025-12-22 | Warnings | 0135-0601-02 0135-0601 00135060102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.