Tylenol Cold Plus Flu Severe Solution
Product Images NDC 50580-403

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Tylenol Cold Plus Flu Severe (NDC 50580-403). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kenvue Brands Llc, 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

Principal Display Panel (Tylenol 01)

TYLENOL COLD PLUS FLU SEVERE dual packaging label featuring a split design: an orange gradient panel labeled DAYTIME with a sun icon, and a dark blue panel labeled NIGHTTIME with a moon and stars icon. The NIGHTTIME panel includes an NDC number. The label is for oral solution dosage form produced by Kenvue Brands LLC.*

FDA Label Image

Principal Display Panel (Tylenol 02)

Label for TYLENOL Cold + Flu + Cough Night 8 fl oz (240 mL) oral solution for adults. Active ingredients include acetaminophen 325 mg, dextromethorphan HBr 10 mg, doxylamine succinate 6.25 mg, and phenylephrine HCl 5 mg per 15 mL. The product is a wild berry burst flavor with 0.7% alcohol, indicated for relief of cold and flu symptoms such as headache, body aches, fever, sore throat, cough, nasal congestion, and runny nose. Distributed by Johnson & Johnson Consumer Inc.*

FDA Label Image

Principal Display Panel (Tylenol 03)

TYLENOL COLD PLUS FLU SEVERE oral solution for adults, 8 fl oz (240 mL), in warming honey lemon flavor. Contains acetaminophen, dextromethorphan HBr, guaifenesin, and phenylephrine HCl. Label shows product name prominently with usage indications including relief for headaches, cough, nasal congestion, and chest congestion. Labeler is Kenvue Brands LLC.*

* 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.