FDA.reportPublic FDA data

NDC 11673-872 - Maximum Strength Daytime Cold and Flu and Nighttime Severe Cold and Flu

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
11673-872
Package NDCs from labels
11673-872-03
Manufacturer
TARGET CORPORATION | TIME CAP LABORATORIES, INC. | MARKSANS PHARMA LIMITED
Effective date
2024-08-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Target Daytime Cold & Flu and Nighttime Severe Cold & Flu LiquidTARGET CORPORATION | TIME CAP LABORATORIES, INC. | MARKSANS PHARMA LIMITED2024-08-22HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-872-03Maximum Strength Daytime Cold and Flu and Nighttime Severe Cold and Flu180 mL in 1 BOTTLESOLUTION180 mL650 mg in 20mL3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-872MAXIMUM STRENGTH DAYTIME COLD AND FLU AND NIGHTTIME SEVERE COLD AND FLU (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, AND ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE,TRIPROLIDINE HYDROCHLORIDE) KIT [TARGET CORPORATION]3Unmatched20240823_0fc523ce-55a7-6384-e063-6394a90aad3f.zip