Equaline Daytime Cold And Flu Relief Solution
Product Images NDC 41163-656

2 FDA label images from United Natural Foods, Inc. Dba Unfi · 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 Equaline Daytime Cold And Flu Relief (NDC 41163-656). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by United Natural Foods, Inc. Dba Unfi, 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

Image 01

Image 01
Equaline daytime and nighttime cold and flu relief combination pack kit features two 12 FL OZ (355 mL) bottles, totaling 24 FL OZ (710 mL). The daytime formulation contains acetaminophen, dextromethorphan HBr, and phenylephrine HCl for non-drowsy relief of aches, fever, sore throat, nasal congestion, and coughs. The nighttime formulation contains acetaminophen, dextromethorphan HBr, and doxylamine succinate for nighttime relief of aches, fever, runny nose, sneezing, and cough. The daytime bottle is alcohol-free and antihistamine-free, while the nighttime bottle contains 10% alcohol. The product is distributed by United Natural Foods, Inc. dba UNFI.*
FDA Label Image

Image 02

Image 02
Drug Facts panels for Equaline Daytime and Nighttime Cold and Flu Relief kit. The Nighttime panel lists active ingredients per 30 mL: Acetaminophen 650 mg, Dextromethorphan HBr 30 mg, and Doxylamine succinate 12.5 mg. The Daytime panel lists active ingredients per 15 mL: Acetaminophen 325 mg, Dextromethorphan HBr 10 mg, and Phenylephrine HCl 5 mg. Both panels include uses, warnings, directions, and other information for safe use.*

* 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.