NDC11 58611097100
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 |
|---|---|
| 58611-0971-0 | 58611-0971 |
| 58611-0971-00 | 58611-0971 |
| 58611-971-00 | 58611-971 |
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 |
|---|---|---|---|---|---|---|
| KinetiCream Pain Relieving Topical Analgesic | MENTHOL | Phoenix Bioperformance Products LLC | bb4c9e73-e62d-4b8c-a16c-b90db1a8b2a7 | 2026-04-06 | Warnings | 58611-971-00 58611-971 58611097100 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.