Cold And Flu Severe Daytime/nighttime Kit
Product Images NDC 76162-823

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Cold And Flu Severe Daytime/nighttime (NDC 76162-823). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Topco Associates 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

Topco-823 (7616282312 1)

TopCare Cold and Flu Severe Daytime/Nighttime Combination Pack carton showing Day Time and Nite Time severe cold and flu relief softgels. The Day Time box contains 12 orange liquid-filled softgels and the Nite Time box contains 12 green liquid-filled softgels, totaling 24 softgels. Active ingredients are Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl for Day Time, and Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl for Nite Time. The labeler is Topco Associates LLC. Warnings, uses, and drug facts panels are visible on the carton sides.*

FDA Label Image

Topco-823 (7616282312 2)

Drug Facts label for Cold and Flu Severe Daytime/Nighttime kit showing active ingredients and purposes for daytime and nighttime softgels, including acetaminophen 325 mg as pain reliever/fever reducer, dextromethorphan HBr as cough suppressant, guaifenesin as expectorant (daytime), doxylamine succinate as antihistamine (nighttime), and phenylephrine HCl as nasal decongestant. The label details uses, warnings including liver and allergy alerts, dosing instructions, inactive ingredients, and storage 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.