Severe Cold And Flu Solution
Product Images NDC 0363-0623

2 FDA label images from Walgreen Company · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Severe Cold And Flu (NDC 0363-0623). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Walgreen Company, 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

Severe Cold & Flu Image 1 (8g00294c3 Image 1)

Severe Cold & Flu Image 1 (8g00294c3 Image 1)
Packaging label for Walgreens Severe Cold & Flu Day & Night Pack oral solution. The pack includes two 12 fl oz (355 mL) bottles, total 24 fl oz (710 mL). The Daytime formula is non-drowsy and contains acetaminophen, dextromethorphan HBr, guaifenesin, and phenylephrine HCl. The Nighttime formula contains acetaminophen, dextromethorphan HBr, doxylamine succinate, and phenylephrine HCl with 10% alcohol. The label highlights maximum strength and is manufactured by Walgreen Company.*
FDA Label Image

Severe Cold & Flu Image 2 (8g00294c3 Image 2)

Severe Cold & Flu Image 2 (8g00294c3 Image 2)
Drug Facts panels for Nighttime Severe Cold & Flu and Daytime Severe Cold & Flu oral solutions. The Nighttime formula contains acetaminophen 650 mg, dextromethorphan HBr 20 mg, doxylamine succinate 12.5 mg, and phenylephrine HCl 10 mg per 30 mL. The Daytime formula contains acetaminophen 325 mg, dextromethorphan HBr 10 mg, guaifenesin 200 mg, and phenylephrine HCl 5 mg per 15 mL. Both panels include uses, warnings, directions, and other information such as storage instructions and sodium content.*

* 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.