Home NDC 55443-0090-2 NDC 55443-0090-2 - VioNex This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 55443-0090
Requested NDC 55443-0090-2
Package NDCs from labels 55443-0090-4, 55443-0090-6, 55443-0090-2, 55443-0090-1
Manufacturer Metrex Research
Effective date 2010-08-17
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type VioNex - Metrex Research Metrex Research 2010-08-17 HUMAN OTC DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 55443-0090-1 VioNex 12 in 1 BOX GEL 12 1 55443-0090-2 VioNex 532 mL in 1 BOTTLE, PLASTIC GEL 532 1 55443-0090-4 VioNex 118 mL in 1 BOTTLE, PLASTIC GEL 118 1 55443-0090-6 VioNex 24 in 1 BOX GEL 24 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55443-0090 VIONEX (CHLOROXYLENOL) GEL [METREX RESEARCH] 1 Legacy NDC, 4 package rows 20100831_86ef8368-867f-4cb3-b44d-21a477a08e40.zip
DailyMed Socrata Ingredients# 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 4 of 12 · 235 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.