Theraflu Severe Cold Relief Nighttime Powder, For Solution
Product Images NDC 50269-101

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Theraflu Severe Cold Relief Nighttime (NDC 50269-101). 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

Inner Label (Inner Label)

Drug Facts panel for THERAFLU SEVERE COLD RELIEF NIGHTTIME powder for solution, honey lemon flavor. Lists active ingredients acetaminophen 650 mg, diphenhydramine HCl 25 mg, and phenylephrine HCl 10 mg with their purposes. Details uses, warnings including liver and allergy warnings, precautions when taking monoamine oxidase inhibitors, and directions for use by age group. Also includes storage and inactive ingredient information, contact information, and lot/licensing data.*

FDA Label Image

Outer Label (Outer Label)

Theraflu Severe Cold Relief Nighttime powder for solution in honey lemon flavor, containing acetaminophen 650 mg and diphenhydramine HCl 25 mg per packet. The label highlights multi-symptom cold relief and hot liquid therapy in a 20-packet carton by JC World Bell Wholesale Co., Inc. The packaging includes drug facts, warnings, directions, and manufacturer information.*

* 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.