NDC11 84126060002
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 |
|---|---|
| 84126-0600-02 | 84126-0600 |
| 84126-0600-2 | 84126-0600 |
| 84126-600-02 | 84126-600 |
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 |
|---|---|---|---|---|---|---|
| Crest Pro-Health Advanced Multi-Protection | SODIUM FLUORIDE | The Procter & Gamble Manufacturing Company | 1cfc5b61-c8e5-943d-e063-6394a90a890b | 2026-04-14 | Warnings | 84126-600-02 84126-600 84126060002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.