Moxe
Product Images NDC 73333-340

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Moxe (NDC 73333-340). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nutrix International, 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

Label (Complete 12oz)

The label for Moxe Citrus Hand Sanitizer by Nutrix International, LLC, contains 70% alcohol. The orange and white label highlights it is made in the USA and is a 12 fl oz (355 ml) bottle. The label also displays drug facts including active ingredient (70% alcohol), purpose (antiseptic), uses, warnings, directions, and inactive ingredients, including water, acrylates copolymer, TEA, glycerin, propylene glycol, and fragrance.*

FDA Label Image

Drug Facts (Drug Facts 12oz)

Drug Facts panel for Moxe by Nutrix International, LLC lists active ingredient as 70% alcohol with antiseptic purpose. It includes uses to reduce skin bacteria, warnings about external use, flammability, eye contact precautions, directions for use, storage info, and a contact number. Inactive ingredients include water, acrylates copolymer, TEA, glycerin, propylene glycol, and fragrance.*

FDA Label Image

Front Label (Front Label 12oz)

Moxe Citrus Hand Sanitizer packaging label showing 70% alcohol content. The label includes branding with the proprietary name MOXE, emphasizes the citrus scent, and indicates the volume as 12 fluid ounces (355 ml). The product is marked as Made in USA and manufactured by Nutrix International, 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.