NDC11 41167093702
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 |
|---|---|
| 41167-0937-02 | 41167-0937 |
| 41167-0937-2 | 41167-0937 |
| 41167-937-02 | 41167-937 |
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 |
|---|---|---|---|---|---|---|
| ACT Anticavity Fluoride Arctic Blast | SODIUM FLUORIDE | Chattem, Inc. | 2d5c1ce7-3c3e-415e-9469-a8d3ddfe2c57 | 2024-08-22 | Warnings | 41167-0937-2 41167-0937 41167093702 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.