Kroger Daytime And Nighttime Cold And Flu Softgel Kit
Product Images NDC 59450-048

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 Kroger Daytime And Nighttime Cold And Flu Softgel (NDC 59450-048). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by The Kroger Co., 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

Kroger Dnkit 2 (59450 048 1)

Kroger Dnkit 2 (59450 048 1)
Drug Facts labels for Kroger DayTime and NightTime Cold and Flu SOFTGEL kit. The Nighttime section details active ingredients acetaminophen 325 mg, dextromethorphan HBr 15 mg, and doxylamine succinate 6.25 mg, with uses, warnings, directions, and inactive ingredients listed. The Daytime section includes acetaminophen 325 mg, dextromethorphan HBr 10 mg, and phenylephrine HCl 5 mg with similar detailed drug facts for use, warnings, and dosage instructions.*
FDA Label Image

Kroger Dnkit 1 (59450 048)

Kroger Dnkit 1 (59450 048)
Kroger DayTime and NightTime Cold and Flu SOFTGEL kit packaging label displays two sets of softgels: DayTime with 32 red softgels and NightTime with 16 green softgels. DayTime ingredients include acetaminophen, dextromethorphan HBr, and phenylephrine HCl; NightTime contains acetaminophen, dextromethorphan HBr, and doxylamine succinate. The label highlights multi-symptom relief and compares active ingredients to Vicks DayQuil/DayQuiL Cold & Flu Relief LiquiCaps. The kit is labeled by The Kroger Co.*

* 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.