Daytime Non Drows Cold And Flu And Nighttime Cold And
Product Images NDC 68210-5015

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 Non Drows Cold And Flu And Nighttime Cold And (NDC 68210-5015). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Spirit Pharmaceuticals 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

Carton (Day Night 24 Ct Combo Back)

Carton (Day Night 24 Ct Combo Back)
Drug Facts label for Daytime Non Drows Cold and Flu and Nighttime Cold and Flu products by Spirit Pharmaceuticals LLC. The label includes active ingredients acetaminophen, dextromethorphan HBr, and doxylamine succinate, categorized separately for daytime and nighttime use. It details purpose, uses, warnings, directions, inactive ingredients, and other drug facts. The label emphasizes keeping out of reach of children and consulting a doctor if necessary.*
FDA Label Image

Day Night 24 Ct Cmdo (Day Night 24 Ct Combo Front)

Day Night 24 Ct Cmdo (Day Night 24 Ct Combo Front)
Packaging label for Daytime Non-Drowsy Cold & Flu and Nighttime Cold & Flu softgels by ValuMeds, labeled by Spirit Pharmaceuticals LLC. The label details active ingredients for Daytime (Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl) and Nighttime (Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate) formulas. It shows 16 orange Daytime and 8 green Nighttime softgel capsules, totaling 24 liquid filled capsules. The label also lists symptom relief details for each type.*

* 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.