NDC11 87228301001
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 |
|---|---|
| 87228-3010-01 | 87228-3010 |
| 87228-3010-1 | 87228-3010 |
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 |
|---|---|---|---|---|---|---|
| Pharmacy Choice | MENTHOL, ZINC OXIDE | PHARMACY CHOICE INC | 5031fc05-e1c7-40b1-e063-6394a90aa12c | 2026-04-24 | Warnings | 87228-3010-1 87228-3010 87228301001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.