Theraflu Expressmax Kit
Product Images NDC 0067-8125

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Theraflu Expressmax (NDC 0067-8125). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Haleon Us Holdings 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

Image 01

Packaging label for Theraflu ExpressMax Severe Cold & Cough value pack containing two 8.3 fl oz (245.5 mL) syrup bottles, total 16.6 fl oz (491 mL). The left bottle is Daytime formula with acetaminophen, dextromethorphan HBr, and phenylephrine HCl, berry flavor, alcohol-free. The right bottle is Nighttime formula with acetaminophen, diphenhydramine HCl, and phenylephrine HCl, also berry flavor and alcohol-free. Labeler is Haleon US Holdings LLC.*

FDA Label Image

Image 02

Theraflu ExpressMax Daytime Severe Cold and Cough syrup label, featuring active ingredients Acetaminophen, Dextromethorphan HBr, and Phenylephrine HCl. The label highlights relief for cough, nasal congestion, sore throat pain, fever, headache, and body ache. Berry flavor, 8.3 fl oz (245.5 mL), alcohol free, with manufacturer Haleon US Holdings LLC.*

FDA Label Image

Image 03

Theraflu ExpressMax Nighttime Severe Cold & Cough syrup, Berry flavor, 8.3 FL OZ (245.5 mL). Active ingredients include Acetaminophen as a pain reliever/fever reducer, Diphenhydramine HCl as an antihistamine/cough suppressant, and Phenylephrine HCl as a nasal decongestant. Alcohol-free formulation, labeled for relief of cough, nasal congestion, sore throat pain, fever, headache, body ache, and runny nose. Labeler: Haleon US Holdings 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.