Goodnow Cold And Flu Day Relief Cold And Flu Night Relief Kit
Product Images NDC 82501-0733

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Goodnow Cold And Flu Day Relief Cold And Flu Night Relief (NDC 82501-0733). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gobrands, 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.

FDA Label Image

Cold & Flu Day Relief, Cold & Flu Night Relief Carton Image 1 (7330236c1 Image 1)

Cold & Flu Day Relief, Cold & Flu Night Relief Carton Image 1 (7330236c1 Image 1)
Goodnow Cold and Flu Day Relief and Cold and Flu Night Relief Kit packaging label. The Day Relief is non-drowsy, contains acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride. The Night Relief is cherry flavored and contains acetaminophen, dextromethorphan hydrobromide, and doxylamine succinate. The kit includes 24 fl oz (2 bottles of 12 fl oz each) and is distributed by Gobrands, Inc.*
FDA Label Image

Cold & Flu Day Relief, Cold & Flu Night Relief Carton Image 2 (7330236c1 Image 2)

Cold & Flu Day Relief, Cold & Flu Night Relief Carton Image 2 (7330236c1 Image 2)
Goodnow Cold and Flu Day Relief and Night Relief Kit packaging label showing drug facts for each. Day Relief contains acetaminophen 325 mg, dextromethorphan HBr 10 mg, and phenylephrine HCl 5 mg in 15 mL doses. Night Relief contains acetaminophen 650 mg, dextromethorphan HBr 30 mg, and doxylamine succinate 12.5 mg in 30 mL doses. The label includes active ingredients, uses, warnings, directions, inactive ingredients, and contact information. Labeler is Gobrands, Inc.*

* 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.