FDA.reportPublic FDA data

NDC 82442-964 - Up and Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold and Cough

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
82442-964
Package NDCs from labels
82442-964-00
Manufacturer
Target Corporation
Effective date
2025-11-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Up and Up Daytime Multi Symptom Severe Cold - Target CorporationTarget Corporation2025-11-24HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82442-964-00Up and Up Daytime Multi Symptom Severe Cold Nighttime Severe Cold and Cough1 in 1 PACKETPOWDER, FOR SOLUTION6650 mg5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82442-964UP AND UP DAYTIME MULTI SYMPTOM SEVERE COLD NIGHTTIME SEVERE COLD AND COUGH (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, DIPHENHYDRAMINE HYDROCHLORIDE) KIT [TARGET CORPORATION]4Unmatched20241016_50ecad33-a2b1-483e-9f03-000caa2af91c.zip