Alka Seltzer Plus Cold Day And Night Effervescent Tablet
Product Images NDC 71992-154

View Photos of 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 Day And Night Effervescent (NDC 71992-154). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincronia Logistica, S.a. De C.v., 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 Package (Inner Package)

Inner Package (Inner Package)
This is a drug information sheet that provides directions and warnings for a medication used for minor aches and pains, cough, sore throat, and fever reduction. It warns against using the drug if the patient is allergic to aspirin or taking certain prescription drugs. It also has warnings for stomach bleeding and Reye's syndrome. The dose varies for adults and children over 12 years of age. The information sheet also includes information about inactive ingredients and sodium content.*
FDA Label Image

Outer Package (Outer Package)

Outer Package (Outer Package)
This is the drug facts section of two Alka-Seltzer PlusĀ® products, Multi-Symptom Cold Day Effervescent Tablets and Multi-Symptom Cold Night Effervescent Tablets. Both products have different active ingredients for different purposes, including aspirin as a pain reliever and fever reducer, dextromethorphan hydrobromide as a cough suppressant, and phenylephrine bitartate as a nasal decongestant. The text also includes warning not to take both products at the same time and some other unreadable texts.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.