Daytime Severe And Nighttime Severe Cold And Flu Kit
Product Images NDC 11673-824

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 11673-824). 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 features two 12 fl oz (355 mL) liquid bottles. The daytime formula contains acetaminophen, dextromethorphan HBr, guaifenesin, and phenylephrine HCl in original flavor. The nighttime formula contains acetaminophen, dextromethorphan HBr, doxylamine succinate, and phenylephrine HCl in berry flavor. Both provide maximum strength cold and flu relief and are alcohol free. Packaging includes product comparisons and warnings.*

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 includes detailed Drug Facts panels for both Daytime Severe and Nighttime Severe formulations listing active ingredients, purposes, uses, warnings, directions, and inactive ingredients. The kit is an over-the-counter product with instructions for dosing and safety information. The label uses primarily orange, white, and black colors with 'daytime severe cold and flu' text on one flap and a barcode on the front panel.*

* 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.