Daytime Nighttime Severe Cold And Flu Relief Kit
Product Images NDC 11822-0328

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 Daytime Nighttime Severe Cold And Flu Relief (NDC 11822-0328). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rite Aid Corporation, 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

Severe Cold And Flu Relief Daytime Nighttime Image 1 (07 01 16 8g00283c2 Image 1)

Severe Cold And Flu Relief Daytime Nighttime Image 1 (07 01 16 8g00283c2 Image 1)
Rite Aid Pharmacy combo pack label featuring Maximum Strength daytime severe cold & flu relief and nighttime severe cold & flu relief oral solutions. Daytime formula contains acetaminophen, phenylephrine HCl, dextromethorphan HBr, and guaifenesin, while nighttime formula contains acetaminophen, dextromethorphan HBr, doxylamine succinate, and phenylephrine HCl. Each solution is 12 FL OZ (355 mL). Daytime is non-drowsy, alcohol and antihistamine free; nighttime contains 10% alcohol. Distributed by Rite Aid Corporation.*
FDA Label Image

Severe Cold And Flu Relief Daytime Nighttime Image 2 (07 01 16 8g00283c2 Image 2)

Severe Cold And Flu Relief Daytime Nighttime Image 2 (07 01 16 8g00283c2 Image 2)
Drug Facts panels for Nighttime Severe Cold & Flu and Daytime Severe Cold & Flu oral solutions. Each panel lists active ingredients with strengths per dose, purposes, uses for relieving cold and flu symptoms, warnings including liver damage risk and allergy alerts, directions by age group, and storage instructions. Sodium content and barcode are 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.