Alka Seltzer Cold Cold And Flu Severe Day Night Fast Dissolve Kit
Product Images NDC 0280-8287

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Alka Seltzer Cold Cold And Flu Severe Day Night Fast Dissolve (NDC 0280-8287). 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

Pdp (Final Artwork (booklet) Asc Cold Flu Severe Dn 24ct Eff)

Drug Facts panels for ALKA SELTZER COLD Cold and Flu Severe Day Night Fast Dissolve kit tablets provide detailed information on active ingredients, directions, uses, warnings, inactive ingredients, and additional precautions. Key active ingredients mentioned include acetaminophen, dextromethorphan hydrobromide, and others. Directions specify dosage limits and administration instructions, while warnings highlight liver risks and allergy alerts. Additional sections address use considerations for specific medical conditions, drug interactions, and when to seek medical advice.*

FDA Label Image

Pdp (Final Artwork (carton) Asc Cold Flu Severe Dn 24ct Eff)

Packaging label for ALKA SELTZER COLD Cold and Flu Severe Day Night Fast Dissolve kit by Bayer HealthCare LLC. The label features a blue and tan color scheme with images of effervescent tablets dissolving in water. It indicates 24 total tablets, including 16 Day non-drowsy tablets with citrus flavor and 8 Night tablets with strawberry honey flavor. The label also lists key symptom relief and contains barcode and manufacturer details.*

* 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.