Alka-seltzer Plus Cold And Flu Tablet, Effervescent
Product Images NDC 85237-2830

2 FDA label images from Select Consumer Group · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Alka-seltzer Plus Cold And Flu (NDC 85237-2830). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Select Consumer Group, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Alkaseltzer (2522830120 Alka Seltzer Plus 2830 2)

Alkaseltzer (2522830120 Alka Seltzer Plus 2830 2)
Alka-Seltzer Plus Severe Cold & Flu PowerFast Fizz effervescent tablets in a 4-tablet multi-pack. The package features a citrus flavor and highlights relief for fever, body aches, cough, nasal congestion, runny nose, and sore throat. Labeler is Select Corporation (repacks from Bayer). Active ingredients include acetaminophen 250 mg, chlorpheniramine maleate 2 mg, dextromethorphan hydrobromide 10 mg, and phenylephrine hydrochloride 5 mg per tablet.*
FDA Label Image

Alkaseltetzer25 (2502832080 Alka Seltzer Plus 2830 4)

Alkaseltetzer25 (2502832080 Alka Seltzer Plus 2830 4)
Alka-Seltzer Plus Cold and Flu effervescent tablets packaging label in citrus flavor. The box highlights severe cold and flu symptom relief with acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, and phenylephrine hydrochloride as active ingredients. It contains 25 pouches with 2 tablets each. Labeler is Select Consumer Group, and the design features blue and orange colors with the Bayer logo.*

* 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.