NDC11 84989001201
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 |
|---|---|
| 84989-0012-01 | 84989-0012 |
| 84989-0012-1 | 84989-0012 |
| 84989-012-01 | 84989-012 |
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 |
|---|---|---|---|---|---|---|
| XIMONTH Quick Essence | SALICYLIC ACID | Shantou Ximonth Biotechnology Co., Ltd. | 4256f607-c9cf-cd0f-e063-6394a90a5487 | 2025-11-26 | Warnings | 84989-012-01 84989-012 84989001201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.