FDA.reportPublic FDA data

NDC 72380-101-10 - VISILAGE RX SILICONE GEL-PAD

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
72380-101
Requested NDC
72380-101-10
Package NDCs from labels
72380-101-10
Manufacturer
Vivera Pharmaceuticals, Inc.
Effective date
2018-12-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
VISILAGE R X SILICONE GEL-PADVivera Pharmaceuticals, Inc.2018-12-04MEDICAL DEVICE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72380-101-10VISILAGE RX SILICONE GEL-PAD2 in 1 BOX21
72380-101-10VISILAGE RX SILICONE GEL-PAD1 in 1 POUCH11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72380-101VISILAGE RX SILICONE GEL-PAD () [VIVERA PHARMACEUTICALS, INC.]12 package rows20190118_d8631cd0-a801-4c5b-a0f4-5e866b2a4d2a.zip

Reported adverse events (FAERS/openFDA)#

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