Daytime And Nighttime Cold And Flu
Product Images NDC 70692-809

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 And Nighttime Cold And Flu (NDC 70692-809). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strive Pharmaceuticals 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

Strive-809 (70692809 74 03)

Strive-809 (70692809 74 03)
Drug Facts panel for DayTime and NightTime Cold and Flu softgels by Strive Pharmaceuticals Inc. The Nighttime softgel contains acetaminophen 325 mg as a pain reliever/fever reducer, dextromethorphan HBr 15 mg as a cough suppressant, and doxylamine succinate 6.25 mg as an antihistamine. The Daytime softgel contains acetaminophen 325 mg for pain relief/fever reduction, dextromethorphan HBr 10 mg as a cough suppressant, and phenylephrine HCl 5 mg as a nasal decongestant. The panel lists uses, warnings, directions, inactive ingredients, and contact information for questions.*
FDA Label Image

Strive-809 (70692809 74 04)

Strive-809 (70692809 74 04)
Packaging label for DayTime and NightTime Cold and Flu by Strive Pharmaceuticals Inc. The DayTime Cold & Flu has 325 mg Acetaminophen, 10 mg Dextromethorphan HBr, and 5 mg Phenylephrine HCL in 32 softgels. The NightTime Cold & Flu contains 325 mg Acetaminophen, 15 mg Dextromethorphan HBr, and 6.25 mg Doxylamine Succinate in 16 softgels. Each variant temporarily relieves common cold and flu symptoms. The label includes dosing facts, warnings, and a barcode with NDC 70692-809.*

* 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.