NDC11 57337018101
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 |
|---|---|
| 57337-0181-01 | 57337-0181 |
| 57337-0181-1 | 57337-0181 |
| 57337-181-01 | 57337-181 |
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 |
|---|---|---|---|---|---|---|
| 3.5OZ MENS DRY ORIGINAL FRESH | ALUMINUM CHLOROHYDRATE | Rejoice International Corp. | 3f6fbc05-f4ad-2f91-e063-6294a90a3e97 | 2025-09-22 | Warnings | 57337-181-01 57337-181 57337018101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.