Nighttime Cold And Flu
Product Images NDC 63868-219

2 FDA label images from Chain Drug Marketing Association Inc. · 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 Nighttime Cold And Flu (NDC 63868-219). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chain Drug Marketing Association Inc., 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 Back (Cdma22 01 Back)

Carton Back (Cdma22 01 Back)
The Nighttime Cold and Flu carton by Chain Drug Marketing Association Inc., NDC 63868-219, displays the drug facts and active ingredients including acetaminophen 325 mg, dextromethorphan HBr 10 mg, doxylamine succinate 6.25 mg, and phenylephrine HCl 5 mg per softgel. It provides uses, warnings, dosage instructions, and storage information. The label advises reading full warnings on the outer carton and notes the product is not manufactured or distributed by Reckitt Benckiser.*
FDA Label Image

Carton Front (Cdma22 01 Front)

Carton Front (Cdma22 01 Front)
Nighttime Cold & Flu Maximum Strength liquid gels packaging label from Quality Choice, a product of Chain Drug Marketing Association Inc. The label highlights fast relief and lists active ingredients: Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, and Phenylephrine HCl. The box contains 16 liquid-filled capsules and is intended for ages 12 and up. The label includes a barcode, NDC 63868-219-16, and tamper-evident packaging information.*

* 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.