Alka-seltzer Plus Cold Day And Night Kit
Product Images NDC 0280-1550

2 FDA label images from Bayer Healthcare Llc. · 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 (NDC 0280-1550). 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.

Product Images & Figures Index

FDA Label Image

Carton Label (430948 86329123 Asp Cold Day Night Eff Tablet 20ct Crtn Dlp R2 Fda2)

Carton Label (430948 86329123 Asp Cold Day Night Eff Tablet 20ct Crtn Dlp R2 Fda2)
The unfolded packaging label for Alka-Seltzer Plus Cold Day and Night Kit by Bayer HealthCare LLC is predominantly blue with white bubbles and features the Alka-Seltzer Plus logo. The label indicates separate sections for day and night effervescent tablets, listing active ingredients including aspirin, dextromethorphan hydrobromide, phenylephrine bitartrate, and doxylamine succinate. The kit contains 12 day and 8 night tablets. Additional elements include dosage form descriptors and a barcode.*
FDA Label Image

Product Carton 2 (85892534 20ct Lbl Day Night Ecl)

Product Carton 2 (85892534 20ct Lbl Day Night Ecl)
Drug Facts panels for Alka-Seltzer Plus Cold Day and Night kit, showing warnings, directions, active and inactive ingredient information, and precautions. The text covers usage instructions for adults and children, potential allergic reactions, medical condition warnings, and advice for pregnant or breastfeeding users. Contact information for questions is also included.*

* 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.