Daytime Cold And Flu Nighttime Cold And Flu Kit
Product Images NDC 79481-5200

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Daytime Cold And Flu Nighttime Cold And Flu (NDC 79481-5200). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meijer, 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

Datime Cold And Flu Nighttime Cold And Flu Image 1 (Image 01)

Daytime Cold and Flu and Nighttime Cold and Flu combo pack by Meijer Distribution Inc featuring two sections: daytime cold & flu in orange with 32 caplets and nighttime cold & flu in blue with 16 caplets. Both products are labeled as maximum strength, multi-symptom treatment for severe cold & flu with active ingredients including acetaminophen, phenylephrine HCl, dextromethorphan HBr, and others. Caplets are shown at actual size.*

FDA Label Image

Daytime Cold And Flu Nighttime Cold And Flu Image 2 (Image 02)

The image shows a product carton label for Meijer Distribution Inc's daytime cold and flu medication branded as 'daytime cold and flu.' The label includes detailed Drug Facts panels listing active ingredients such as Acetaminophen 325 mg, Dextromethorphan HBr 10 mg, Guaifenesin 200 mg, and Phenylephrine HCl 5 mg per caplet. It also contains warnings, directions, and usage instructions for temporary relief of cold and flu symptoms. The label highlights parent and product-specific warnings, dosage information by age group, and inactive ingredients.*

* 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.