NDC11 61577310301
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 |
|---|---|
| 61577-3103-01 | 61577-3103 |
| 61577-3103-1 | 61577-3103 |
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 |
|---|---|---|---|---|---|---|
| SOMBRA COOL THERAPY | MENTHOL | SOMBRA COSMETICS INC. | 87e9b16b-1cab-48f7-b9e4-1c3eaeeb3ca3 | 2026-04-21 | Warnings | 61577-3103-1 61577-3103 61577310301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.