Daytime Mucus Relief Severe Cold And Nighttime Cold And Flu
Product Images NDC 11673-463

1 FDA label image from Target Corporation · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Daytime Mucus Relief Severe Cold And Nighttime Cold And Flu (NDC 11673-463). 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.

Product Images & Figures Index

FDA Label Image

Acetaminophen 650 mg, Diphenhydramine Hci 25 mg, Phenylephrine Hci 10 mg Acetaminophen 650 mg, Dextromethorphan Hbr 20 mg Guaifenesin 400 mg Phenylephrine Hci 10 mg (Mucus Relief Severe Cold And Mucus Relief Nighttim 1)

Acetaminophen 650 mg, Diphenhydramine Hci 25 mg, Phenylephrine Hci 10 mg Acetaminophen 650 mg, Dextromethorphan Hbr 20 mg Guaifenesin 400 mg Phenylephrine Hci 10 mg (Mucus Relief Severe Cold And Mucus Relief Nighttim 1)
The packaging label for up&up maximum strength Daytime Severe Cold and Nighttime Cold and Flu liquid medicines contains two 6 fl oz (177 mL) bottles, totaling 12 fl oz (354 mL). The daytime formula includes acetaminophen, dextromethorphan HBr, guaifenesin, and phenylephrine HCl for ages 12 and older. The nighttime formula includes acetaminophen, diphenhydramine HCl, and phenylephrine HCl. The label details active ingredients, purposes, warnings, uses, and directions with NDC 11673-463-12, distributed by TARGET Corporation.*

* 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.