NDC 69626-0011 - Easy 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
69626-0011
Package NDCs from labels
69626-0011-5
Manufacturer
Leosons Overseas Corp | Ultra Seal Corporation
Effective date
2016-12-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Easy Gel - Leosons Overseas Corp | Ultra Seal CorporationLeosons Overseas Corp | Ultra Seal Corporation2016-12-14MEDICAL DEVICE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69626-0011-5Easy Gel113.4 g in 1 TUBEGEL113.41

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69626-0011EASY GEL (STERILE LUBRICATING JELLY) GEL [LEOSONS OVERSEAS CORP]11 package rows20161229_2a9a3aba-d3e0-4fd2-a3f7-535d25fba4eb.zip

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 27 of 27 · 521 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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