Basic Care Nighttime Cold And Flu Capsule, Liquid Filled
Product Images NDC 72288-056

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 Basic Care Nighttime Cold And Flu (NDC 72288-056). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amazon.com Services Llc, 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

Daytime Cold And Flu Nighttime Cold And Flu Image 1 (Image 01)

Daytime Cold And Flu Nighttime Cold And Flu Image 1 (Image 01)
The packaging label for basic care daytime cold and flu and nighttime cold and flu kit by Amazon. The label highlights two products: Daytime Cold & Flu with acetaminophen, dextromethorphan HBr, and phenylephrine HCl in 32 softgels, and Nighttime Cold & Flu with acetaminophen, dextromethorphan HBr, and doxylamine succinate in 16 softgels. Both offer multi-symptom relief and are alcohol free.*
FDA Label Image

Daytime Cold And Flu Nighttime Cold And Flu Image 2 (Image 02)

Daytime Cold And Flu Nighttime Cold And Flu Image 2 (Image 02)
Basic Care Daytime Cold and Flu Nighttime Cold and Flu Kit packaging label. The kit includes two drug facts panels describing the active ingredients: acetaminophen 325 mg, dextromethorphan HBr (15 mg Nighttime, 10 mg Daytime), doxylamine succinate 6.25 mg, and phenylephrine HCl 5 mg. The label outlines uses, warnings, directions, and other drug facts. It is labeled by Amazon.com Services LLC and features an orange and blue color scheme with bar code, tamper-evident information, and a convenient reclosable tab.*

* 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.