Tylenol Cold Plus Flu Tablet, Film Coated
Product Images NDC 53209-1003

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 Plus Flu (NDC 53209-1003). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Morning Star Otc, 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 (Tylenol Col Flu 2 Tablets)

Label (Tylenol Col Flu 2 Tablets)
TYLENOL Cold Plus Flu Severe 2 caplets film-coated oral tablets packaging label. The product contains Acetaminophen 325 mg, Dextromethorphan HBr 10 mg, Guaifenesin 200 mg, and Phenylephrine HCl 5 mg per caplet. Distributed by Johnson & Johnson Consumer Inc., repackaged by Morning Star OTC. The label includes a drug facts panel outlining active ingredients, uses, warnings, and directions for use. The package is red with white and yellow text, featuring the TYLENOL logo prominently.*
FDA Label Image

Label (Tylenol Col Flu 25 Pouches)

Label (Tylenol Col Flu 25 Pouches)
Packaging label for TYLENOL Cold Plus Flu Severe tablets, film coated, for oral use. The label lists active ingredients acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride. The package contains 25 pouches with 2 caplets each. It is repackaged by Morning Star OTC in Los Angeles. The label also includes warnings, directions, and a contact phone number for TYLENOL consumer support.*

* 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.