Home NDC 72401-025 NDC 72401-025 - Solox Gel 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 72401-025
Package NDCs from labels 72401-025-45
Manufacturer Solus Rx, LLC
Effective date 2019-02-06
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Solox Gel - Solus Rx, LLC Solus Rx, LLC 2019-02-06 PRESCRIPTION MEDICAL DEVICE LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72401-025-45 Solox Gel 45 mL in 1 TUBE 45 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72401-025 SOLOX GEL () [SOLUS RX, LLC] 1 1 package rows 20190207_9d7471cb-019d-4862-bd18-34a2cafe74ea.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.