Daytime Nighttime Cold And Flu Kit
Product Images NDC 0363-0567

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 Daytime Nighttime Cold And Flu (NDC 0363-0567). 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

5670294c5 Image 1

5670294c5 Image 1
Daytime Nighttime Cold and Flu kit by Walgreens features a day formula labeled as non-drowsy with acetaminophen 650 mg, dextromethorphan HBr 30 mg/30mL, phenylephrine HCl 12.5 mg/30mL for pain relief, fever, cough, and nasal congestion. The nighttime formula contains acetaminophen, dextromethorphan HBr, doxylamine succinate, indicated for similar symptoms plus sneezing and runny nose, with 10% alcohol. The kit includes two 12 fl oz (355 mL) bottles totaling 24 fl oz (710 mL).*
FDA Label Image

5670294c5 Image 2

5670294c5 Image 2
Drug Facts text panel for Walgreen Company's Daytime Nighttime Cold and Flu OTC kit. The panel details active ingredients, uses, warnings, directions, and other drug facts for the Nighttime Cold & Flu (per 30 mL) and Daytime Cold & Flu (per 15 mL) formulations. Nighttime contains acetaminophen 650 mg, dextromethorphan HBr 30 mg, and doxylamine succinate 12.5 mg. Daytime contains acetaminophen 325 mg, dextromethorphan HBr 10 mg, and phenylephrine HCl 5 mg. It provides standard OTC warnings, usage instructions by age group, and dosage limits.*

* 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.