Cold And Flu Solution
Product Images NDC 0363-0566

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 Cold And Flu (NDC 0363-0566). 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

Walgreens Cold And Flu Image 1 (7330294c2 Image 1)

Walgreens Cold And Flu Image 1 (7330294c2 Image 1)
Daytime Nighttime Cold and Flu kit by Walgreens features two 12 fl oz (355 mL) bottles. The daytime formula is non-drowsy and contains acetaminophen, dextromethorphan HBr, and phenylephrine HCl for aches, fever, sore throat, cough, and nasal congestion. The nighttime formula contains acetaminophen, dextromethorphan HBr, and doxylamine succinate with 10% alcohol for aches, fever, sore throat, cough, sneezing, and runny nose, with cherry flavor.*
FDA Label Image

Walgreens Cold And Flu Image 2 (7330294c2 Image 2)

Walgreens Cold And Flu Image 2 (7330294c2 Image 2)
Drug Facts panels for Walgreen Company's daytime nighttime cold and flu kit. The Nighttime Cold & Flu section lists active ingredients acetaminophen 650 mg, dextromethorphan HBr 30 mg, and doxylamine succinate 12.5 mg per 30 mL, with purposes and warnings for use. The Daytime Cold & Flu section lists acetaminophen 325 mg, dextromethorphan HBr 10 mg, and phenylephrine HCl 5 mg per 15 mL, along with corresponding purposes, warnings, and directions for use. Additional information on sodium content and storage conditions is included.*

* 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.