NDC 59088-435-10
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
- 59088-435-10
- Product root
- 59088-435
- Identity scope
- Package
- Primary current NDC product row
- Not present
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 59088-435 | 59088-435-10 | I | Inactivated by FDA | 2026-08-03 |
openFDA label cross-check#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Lextol | DICLOFENAC SODIUM, CAPSAICIN | PureTek Corporation | 042765e5-bd75-8224-e063-6394a90a141b | 2025-12-19 | Boxed warning, Warnings, Adverse reactions | 59088-435-10 59088043510 |
| Diclogen | DICLOFENAC SODIUM, CAMPHOR AND MENTHOL | PureTek Corporation | 1e2bb4e5-bb65-48a0-e063-6294a90a54d1 | 2025-12-18 | Boxed warning, Warnings, Adverse reactions | 59088-435-10 59088043510 |
| Lixofen | DICLOFENAC SODIUM, KINESIOLOGY TAPE | PureTek Corporation | 1e2a687b-a838-9b16-e063-6394a90a69f3 | 2025-12-18 | Boxed warning, Warnings, Adverse reactions | 59088-435-10 59088043510 |