FDA.reportPublic FDA data

NDC 11822-1226 - Ear Wax Removal System Rite Aid

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
11822-1226
Package NDCs from labels
11822-1226-1
Manufacturer
Rite Aid | Product Quest Mfg
Effective date
2018-06-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ear Wax Removal Drops Rite Aid - Rite Aid | Product Quest MfgRite Aid | Product Quest Mfg2018-06-13HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-1226-1Ear Wax Removal SystemRite Aid15 mL in 1 BOTTLESOLUTION/ DROPS15 mL6.5 g in 100mL1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-1226EAR WAX REMOVAL SYSTEM RITE AID (CARBAMIDE PEROXIDE - 6.50%) KIT [RITE AID]1Unmatched20180613_0a7e2ef1-14a0-44b0-a9ca-0db89b8efbc4.zip