Daytime Ultra Concentrated Cold And Flu Capsule, Liquid Filled
Product Images NDC 11673-843

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 Daytime Ultra Concentrated Cold And Flu (NDC 11673-843). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Target Corporation, 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

777t-target-daytimesoftgels-48s-ifc 1 (777t Target Daytimesoftgels 48s Ifc 1)

777t-target-daytimesoftgels-48s-ifc 1 (777t Target Daytimesoftgels 48s Ifc 1)
The packaging label for Daytime Ultra Concentrated Cold and Flu capsules, liquid filled, maximum strength, by Target Corporation. The front displays active ingredients acetaminophen 325 mg, dextromethorphan HBr 10 mg, and phenylephrine HCl 5 mg. The design is orange with yellow and white text, with a window showing 48 softgels. The label includes drug facts, usage warnings, dosage directions, and a bar code.*
FDA Label Image

777t-dtultra-48s-label (777t Dtultra 48s Label)

777t-dtultra-48s-label (777t Dtultra 48s Label)
Packaging label for Daytime Ultra Concentrated Cold and Flu softgels containing Acetaminophen 325 mg, Dextromethorphan HBr 10 mg, and Phenylephrine HCl 5 mg per softgel. The label indicates 48 softgels per container and lists Target Corporation as the labeler. The design features an orange background with yellow and white text detailing active ingredients and typical cold and flu symptoms addressed by the product.*

* 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.