NDC11 50804021148
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 |
|---|---|
| 50804-0211-48 | 50804-0211 |
| 50804-211-48 | 50804-211 |
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 |
|---|---|---|---|---|---|---|
| GOODSENSE Maximum Strength Medicated | WITCH HAZEL | GEISS, DESTIN & DUNN, INC | 5453a12b-e775-4101-bd3a-337857e9e167 | 2025-12-05 | Warnings | 50804-211-48 50804-211 50804021148 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.