NDC11 87860000200
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 |
|---|---|
| 87860-0002-0 | 87860-0002 |
| 87860-0002-00 | 87860-0002 |
| 87860-002-00 | 87860-002 |
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 |
|---|---|---|---|---|---|---|
| Meriwether Skin Pain Relief | MENTHOL, UNSPECIFIED FORM | Meriwether Skin LLC | f6e155be-5879-4176-bb0e-e364f2e5cdf9 | 2026-07-16 | Warnings | 87860-002-00 87860-002 87860000200 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.