NDC 83559-017

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
83559-017
Product root
83559-017
Identity scope
Product
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 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct83559-017EExcluded after deficient or non-compliant submission was not corrected2026-10-02
excluded packagepackage83559-01783559-017-01EExcluded after deficient or non-compliant submission was not corrected2026-10-02
excluded packagepackage83559-01783559-017-02EExcluded after deficient or non-compliant submission was not corrected2026-10-02

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ENOKON PAIN RELIEF CreamPAIN RELIEF CREAMHenan Enokon Medical Instrument Co., Ltd.567502df-d5f0-a3f7-e063-6394a90a57f02026-07-12WarningsExact identifier
ndc (product): 83559-017

Reported adverse events (FAERS/openFDA)#

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