Alka-seltzer Plus Maximum Strength Severe Sinus Congestion And Cough Day And Night Kit
Product Images NDC 0280-1610

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Alka-seltzer Plus Maximum Strength Severe Sinus Congestion And Cough Day And Night (NDC 0280-1610). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bayer Healthcare 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

Carton 20 Count 1 (85740989 20ct Ctn1)

Alka-Seltzer Plus Maximum Strength Severe Sinus Congestion and Cough Day and Night oral kit by Bayer HealthCare LLC. The label shows a dual formulation with Day and Night liquid gel capsules. The Day section includes acetaminophen, dextromethorphan HBr, and phenylephrine HCl for symptom relief. The Night section adds doxylamine succinate to the mix. The package contains 12 Day and 8 Night liquid gel capsules.*

FDA Label Image

Carton 20 Count 2 (85740989 20ct Ctn2)

Drug Facts panels for Alka-Seltzer Plus Maximum Strength Severe Sinus Congestion and Cough Day and Night Liquid Gels, with separate sections for Day and Night formulations. Panels detail active ingredients (acetaminophen 325 mg, dextromethorphan hydrobromide, doxylamine succinate for night, phenylephrine hydrochloride), uses, warnings including liver and allergy alerts, sore throat warnings, do not use conditions, and instructions to ask a doctor or pharmacist before use under specific health conditions or medication.*

FDA Label Image

Carton 20 Count 3 (85740989 20ct Ctn3)

Packaging label for Alka-Seltzer Plus Maximum Strength Severe Sinus Congestion and Cough Day and Night Kit. The label includes drug facts and directions for both day and night liquid gels, highlighting warnings, dosing information, inactive ingredients, and storage instructions. The label is color-coded blue for day and green for night liquid gels and displays the Bayer HealthCare LLC manufacturer information, a barcode, and a parental warning about teen medicine abuse.*

* 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.