Combination Pack Hyvee Daytime And Nighttime Severe Cold And Flu Softgel - 24ct Kit
Product Images NDC 42507-106

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Combination Pack Hyvee Daytime And Nighttime Severe Cold And Flu Softgel - 24ct (NDC 42507-106). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hyvee Inc, 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

Daytime&nightime Cold&flu (42507106 3)

COMBINATION PACK HyVee Daytime and Nighttime Severe Cold and Flu SOFTGEL contains two sets of softgels, each with 12 count. The daytime formula includes acetaminophen 325 mg, dextromethorphan HBr 10 mg, guaifenesin 200 mg, and phenylephrine HCl 5 mg. The nighttime formula includes acetaminophen 325 mg, dextromethorphan HBr 10 mg, doxylamine succinate 6.25 mg, and phenylephrine HCl 5 mg. The pack is labeled by HyVee Inc and features distinct orange and blue sections for day and night formulations.*

FDA Label Image

Daytime&nightime Cold&flu2 (42507106 4)

Drug Facts label for COMBINATION PACK HyVee Daytime and Nighttime Severe Cold and Flu SOFTGEL kit. The label details active ingredients and purposes for daytime and nighttime softgels, lists uses, warnings including liver warning and allergy alert, and advises consulting a doctor before use for certain conditions. Directions for use, inactive ingredients, overdose warnings, and storage instructions are included. Customer service contact information is provided.*

* 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.