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)
Drug Facts panels for ALKA SELTZER PLUS Cold Day and Night Effervescent tablets, covering warnings, directions, ingredients, and usage instructions. Information includes allergy warnings, stomach bleeding warnings, precautions for children and pregnant or breastfeeding women, dosing instructions for adults and children 12 years and older, inactive ingredients, as well as advice to consult a doctor in certain conditions. Contact information and storage instructions are also provided.*
FDA Label Image

Outer Package (Outer Package)

Outer Package (Outer Package)
Front and sides of the ALKA SELTZER PLUS Cold Day and Night Effervescent tablets box by Bayer, featuring distinct panels for Day (non-drowsy) and Night formulations with 8 and 12 effervescent tablets respectively. The packaging highlights multi-symptom cold relief and includes drug facts with active ingredients aspirin, dextromethorphan hydrobromide, and phenylephrine bitartrate. Label includes lot, expiry date sections, and a barcode.*

* 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.