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#

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.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	59088-435	59088-435-10	I	Inactivated by FDA		2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	59088-435	59088-435-10	I	Inactivated by FDA		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	59088-435	59088-435-10	I	Inactivated by FDA		excluded / ndc_excluded.zip	`f5e01cc5f278…`	`a2eaf40c39c3…`

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.

Matched openFDA labels page 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
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	Exact identifier ndc (package): 59088-435-10 ndc11 (package): 59088043510
Diclogen	DICLOFENAC SODIUM, CAMPHOR AND MENTHOL	PureTek Corporation	1e2bb4e5-bb65-48a0-e063-6294a90a54d1	2025-12-18	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 59088-435-10 ndc11 (package): 59088043510
Lixofen	DICLOFENAC SODIUM, KINESIOLOGY TAPE	PureTek Corporation	1e2a687b-a838-9b16-e063-6394a90a69f3	2025-12-18	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 59088-435-10 ndc11 (package): 59088043510

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.