Daytime Severe And Nighttime Severe Cold And Flu Kit
Product Images NDC 11673-739

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Daytime Severe And Nighttime Severe Cold And Flu (NDC 11673-739). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Target Corporation, 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

Daytime Nighttime Severe Cold And Flu Image 1 (Image 01)

Daytime Severe and Nighttime Severe Cold and Flu kit from Target Corporation featuring two 12 FL OZ (355 mL) liquid bottles. The Daytime Severe contains acetaminophen, dextromethorphan HBr, guaifenesin, and phenylephrine HCl with original flavor. The Nighttime Severe contains acetaminophen, dextromethorphan HBr, doxylamine succinate, and phenylephrine HCl with berry flavor. Both are labeled as max strength, alcohol free, and for relief of cold and flu symptoms.*

FDA Label Image

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

Packaging label for Daytime Severe and Nighttime Severe cold and flu kit by Target Corporation. The label presents detailed drug facts for both Daytime Severe (acetaminophen, dextromethorphan HBr, guaifenesin) and Nighttime Severe (acetaminophen, dextromethorphan HBr, doxylamine succinate) formulations, including active ingredients, purposes, uses, warnings, directions, and inactive ingredients. The label is predominantly orange and white with black text and an up&up logo.*

* 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.