NDC11 85162000203
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 |
|---|---|
| 85162-0002-03 | 85162-0002 |
| 85162-0002-3 | 85162-0002 |
| 85162-002-03 | 85162-002 |
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 |
|---|---|---|---|---|---|---|
| AMERFRESH FLUORIDE | SODIUM FLUORIDE | Yangzhou ONE & ONLY Personal Care Products Co., LTD | 827e45bb-84c0-48ee-a60b-2cc32b8f33e3 | 2025-01-16 | Warnings | 85162-002-03 85162-002 85162000203 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.