Tylenol Cold Flu Severe Tablet, Film Coated
Product Images NDC 50269-550

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Tylenol Cold Flu Severe (NDC 50269-550). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Jc World Bell Wholesale Co., 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

Label (Label)

Label (Label)
This is the packaging label for Tylenol Cold Flu Severe, a film-coated tablet for oral use. The label highlights active ingredients including acetaminophen, dextromethorphan HBr, phenylephrine HCl, and guaifenesin. The package contains 20 pouches, each with 2 caplets. The label features red and blue colors, and mentions relief for head and body aches, fever, sore throat, cough, nasal congestion, and mucus/chest congestion. It is labeled for adult use and distributed by JC World Bell Wholesale Co., Inc.*
FDA Label Image

Pouch Label (Pouch Label)

Pouch Label (Pouch Label)
This image shows multiple drug facts panels for Tylenol Cold + Flu Severe tablets. The panels include active ingredients acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride with their respective dosages. The text covers uses, warnings, directions, and other regulatory information for the oral film-coated tablets, labeled for adult use and from JC World Bell Wholesale Co., Inc.*

* 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.