NDC11 81277000402
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 |
|---|---|
| 81277-0004-02 | 81277-0004 |
| 81277-0004-2 | 81277-0004 |
| 81277-004-02 | 81277-004 |
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 |
|---|---|---|---|---|---|---|
| Sure Regular Original Solid | ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY | Sodalis USA LLC | a6c0a118-0d8c-4d29-b015-cf3ff47f1229 | 2024-11-08 | Warnings | 81277-004-02 81277-004 81277000402 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.