NDC11 10157210303
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 |
|---|---|
| 10157-2103-03 | 10157-2103 |
| 10157-2103-3 | 10157-2103 |
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 |
|---|---|---|---|---|---|---|
| Tucks Medicated Cooling Pads | WITCH HAZEL | Blistex Inc | b3e68008-3d0d-4124-9579-b503e9fb95c9 | 2024-12-13 | Warnings | 10157-2103-3 10157-2103 10157210303 |
| Tucks Medicated Cooling Pads | WITCH HAZEL | Blistex Inc | 1eb3c742-7104-7b47-e063-6394a90a84ba | 2024-08-02 | Warnings | 10157-2103 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.