NDC11 41167097901
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 |
|---|---|
| 41167-0979-01 | 41167-0979 |
| 41167-0979-1 | 41167-0979 |
| 41167-979-01 | 41167-979 |
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 Restoring Anticavity Fluoride Mint Burst | SODIUM FLUORIDE | Chattem, Inc. | a38363e6-7105-4663-95a0-09ecb2948f83 | 2025-09-30 | Warnings | 41167-0979-1 41167-0979 41167097901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.