NDC 10157-2103-7
This exact product or package identity exists in FDA auxiliary data but is not present in the current primary NDC product table. The package identity is preserved; status rows are reported source observations, not medical conclusions.
- Requested NDC
- 10157-2103-7
- Product root
- 10157-2103
- Identity scope
- Package
- Primary current NDC product row
- Not present
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 10157-2103 | 10157-2103-7 | D | Discontinued by firm | 2026-08-03 |
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 |
| Tucks Medicated Cooling Pads | WITCH HAZEL | Blistex Inc | 1eb3c742-7104-7b47-e063-6394a90a84ba | 2024-08-02 | Warnings | 10157-2103 |