Alka-seltzer Plus Day Severe Cold Plus Flu Powder, For Solution
Product Images NDC 0280-0921

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Alka-seltzer Plus Day Severe Cold Plus Flu (NDC 0280-0921). 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

431296 C7506 Asp Severe Cold Flu Day Powder Ctn Fda1reduced

Alka-Seltzer Plus Day Severe Cold Plus Flu powder for solution packaging label. The label features the Alka-Seltzer Plus logo with indication for severe cold and flu symptoms. It specifies the honey lemon zest flavor and contains 6 packets. Active ingredients include acetaminophen 500 mg, dextromethorphan hydrobromide 20 mg, guaifenesin 400 mg, and phenylephrine hydrochloride 10 mg per packet. The product is labeled as non-drowsy and for oral use, manufactured by Bayer HealthCare 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.