Axim Daytime - Night Time 48 Softgels
Product Images NDC 82706-003

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Axim Daytime - Night Time 48 Softgels (NDC 82706-003). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vivunt Pharma 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

Axim Daytime Night Time 48 Caps

Axim Daytime Night Time 48 Caps
AXIM DayTime - Night Time 48 Softgels carton by VIVUNT PHARMA LLC, featuring a split design with DayTime in orange and NightTime in blue. The box contains 32 DayTime softgels and 16 NightTime softgels. DayTime is for cold and flu relief with acetaminophen, dextromethorphan HBr, and phenylephrine HCl. NightTime provides nighttime relief with acetaminophen, dextromethorphan HBr, and doxylamine succinate. Both sections list multi-symptom relief uses including pain and fever reduction, cough suppression, and congestion relief.*
FDA Label Image

Axim Daytime Night Time 72 Caps

Axim Daytime Night Time 72 Caps
The packaging label for AXIM DayTime - Night Time 48 Softgels features a combined orange and blue design. The DayTime section (orange) highlights non-drowsy cold and flu multi-symptom relief softgels (48 count) containing acetaminophen, dextromethorphan HBr, and phenylephrine HCl. The NightTime section (blue) offers nighttime relief softgels (24 count) with acetaminophen, dextromethorphan HBr, and doxylamine succinate. Both sections list pain reliever, fever reducer, cough suppressant, and nasal decongestant or antihistamine benefits. The labeler is VIVUNT PHARMA LLC.*

* 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.