Nitetime Cold And Flu Solution
Product Images NDC 41250-459

2 FDA label images from Meijer Distribution Inc · 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 Nitetime Cold And Flu (NDC 41250-459). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meijer Distribution 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

733026ec5 Image 1

733026ec5 Image 1
Daytime Nitetime Cold and Flu combo pack by Meijer Distribution Inc. This OTC kit contains two 12 FL OZ (355 mL) liquid formulations: a non-drowsy daytime formula with acetaminophen, dextromethorphan HBr, and phenylephrine HCl, and a nighttime formula with acetaminophen, dextromethorphan HBr, and doxylamine succinate in cherry flavor. The daytime relief is alcohol and antihistamine free, while the nighttime contains 10% alcohol.*
FDA Label Image

733026ec5 Image 2

733026ec5 Image 2
Drug Facts panels for Nighttime Cold & Flu and Daytime Cold & Flu liquid formulations in a kit. The Nighttime panel lists active ingredients including Acetaminophen 650 mg, Dextromethorphan HBr 30 mg, and Doxylamine succinate 12.5 mg per 30 mL dose with uses, warnings, directions, and other information. The Daytime panel lists active ingredients including Acetaminophen 325 mg, Dextromethorphan HBr 10 mg, and Phenylephrine HCl 5 mg per 15 mL dose with similar detailed usage and safety instructions. Both panels emphasize proper dosing and storage instructions.*

* 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.