Daytime Nighttime Severe Cold And Flu Kit
Product Images NDC 0363-0746

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Daytime Nighttime Severe Cold And Flu (NDC 0363-0746). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Walgreens, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

627t Wg Severe Coldflu Ifc 24s

The packaging label for Walgreens Daytime Nighttime Severe Cold & Flu Maximum Strength kit features a dual-color design with an orange section labeled 'Daytime Severe Cold & Flu' containing 16 softgels and a blue section labeled 'Nighttime Severe Cold & Flu' containing 8 softgels. The daytime formula includes acetaminophen, dextromethorphan HBr, guaifenesin, and phenylephrine HCl. The nighttime formula adds doxylamine succinate and also contains acetaminophen, dextromethorphan HBr, and phenylephrine HCl. Both are liquid-filled softgels. The front and back panels include detailed drug facts, uses, warnings, and dosing directions for each separate formulation. The labeler is Walgreens, and the total quantity is 24 softgels.*

FDA Label Image

627t Wg Severe Coldflu Ifc 48s

Packaging label for DAYTIME NIGHTTIME SEVERE COLD AND FLU Maximum Strength kit by Walgreens. The kit contains 32 daytime softgels and 16 nighttime softgels. Daytime softgels contain acetaminophen 325 mg, dextromethorphan HBr 10 mg, guaifenesin 200 mg, and phenylephrine HCl 5 mg. Nighttime softgels contain acetaminophen 325 mg, dextromethorphan HBr 10 mg, doxylamine succinate 6.25 mg, and phenylephrine HCl 5 mg. The label includes drug facts, warnings, directions, and a 100% satisfaction guarantee. Total 48 softgels.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.