Daytime Nighttime Sinus Relief Kit
Product Images NDC 69842-908

1 FDA label image from Cvs Pharmacy · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Daytime Nighttime Sinus Relief (NDC 69842-908). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cvs Pharmacy, 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

Acetaminophen 325 mg, Dextromethorphan Hbr 10 mg, Guaifenesin 200 mg, Phenylephrine HCl 5 mg, Acetaminophen 325 mg, Dextromethorphan Hbr 10 mg, Doxylamine Succinate 6.25 mg, Phenylephrine HCl 5 mg (Mucus Relief Daytime Sinus Nighttime Sinus Softgel 1)

Acetaminophen 325 mg, Dextromethorphan Hbr 10 mg, Guaifenesin 200 mg, Phenylephrine HCl 5 mg, Acetaminophen 325 mg, Dextromethorphan Hbr 10 mg, Doxylamine Succinate 6.25 mg, Phenylephrine HCl 5 mg (Mucus Relief Daytime Sinus Nighttime Sinus Softgel 1)
The Daytime Nighttime Sinus Relief Maximum Strength Kit by CVS Pharmacy is an oral OTC drug pack containing 16 daytime softgels and 8 nighttime softgels, total 24 softgels. The daytime formulation includes acetaminophen 325 mg, dextromethorphan HBr 10 mg, guaifenesin 200 mg, and phenylephrine HCl 5 mg. The nighttime formulation contains acetaminophen 325 mg, dextromethorphan HBr 10 mg, doxylamine succinate 6.25 mg, and phenylephrine HCl 5 mg. The packaging provides detailed Drug Facts, indications, warnings, directions, and inactive ingredients for both formulations.*

* 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.