NDC11 83013033910
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 |
|---|---|
| 83013-0339-10 | 83013-0339 |
| 83013-339-10 | 83013-339 |
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 |
|---|---|---|---|---|---|---|
| Strawberry Flavor Sodium Fluoride Anticavity Toothpast | SODIUM FLUORIDE | HISMILE PTY LTD | 426c2aca-ca2b-5e34-e063-6294a90ae37c | 2025-11-02 | Warnings | 83013-339-10 83013-339 83013033910 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.