NDC11 10356012004
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 |
|---|---|
| 10356-0120-04 | 10356-0120 |
| 10356-0120-4 | 10356-0120 |
| 10356-120-04 | 10356-120 |
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 |
|---|---|---|---|---|---|---|
| Aquaphor Itch Relief | HYDROCORTISONE | Beiersdorf Inc | b1d0333f-ba60-35d8-e053-2995a90af932 | 2025-12-16 | Warnings | 10356-120-04 10356-120 10356012004 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.