FDA.reportPublic FDA data

NDC 69842-617 - MAXIMUM STRENGTH DAYTIME NIGHTTIME SINUS RELIEF

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
69842-617
Package NDCs from labels
69842-617-16
Manufacturer
CVS Pharmacy, Inc. | TIME CAP LABORATORIES, INC. | MARKSANS PHARMA LIMITED
Effective date
2026-03-26
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
630T CVS 69842-442 MAXIMUM STRENGTH DAYTIME NIGHTTIME SINUS RELIEFCVS Pharmacy, Inc. | TIME CAP LABORATORIES, INC. | MARKSANS PHARMA LIMITED2026-03-26HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-617-16MAXIMUM STRENGTH DAYTIME NIGHTTIME SINUS RELIEF16 in 1 BLISTER PACKCAPSULE, LIQUID FILLED165 mg4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-617MAXIMUM STRENGTH DAYTIME NIGHTTIME SINUS RELIEF (ACETAMINOPHEN DEXTROMETHORPHAN HBR GUAIFENESIN PHENYLEPHRINE HCL AND ACETAMINOPHEN DEXTROMETHORPHAN HBR DOXYLAMINE SUCCINATE PHENYLEPHRINE HCL) KIT [CVS PHARMACY, INC.]3Unmatched20250215_c17d5ba7-3302-7931-e053-2a95a90a5a6c.zip