Hand Sanitizer
Product Images NDC 74105-900

3 FDA label images from Deviation Distilling Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 74105-900). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Deviation Distilling 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

3oz (3oz Bottle Label)

3oz (3oz Bottle Label)
Label for Hand Sanitizer Non-Sterile Solution by Deviation Distilling LLC. The label states 80% alcohol antiseptic topical solution with a volume of 3 fl oz (88.72 mL). The label includes the company address in Denver, CO, and website. A partial Drug Facts panel on the right details the active ingredient, use, warnings, directions, storage, and inactive ingredients.*
FDA Label Image

8oz (8oz Bottle Label2)

8oz (8oz Bottle Label2)
Label for Hand Sanitizer Non-Sterile Solution by Deviation Distilling. It is an 80% alcohol antiseptic topical solution in an 8 fl oz (240 mL) container. The label includes the manufacturer's address in Denver, CO, and the website www.deviationdistilling.com. The label also features sections of drug facts including active ingredient, uses, warnings, directions, and other information.*
FDA Label Image

Gallon (Hand Sanitizer Gallon)

Gallon (Hand Sanitizer Gallon)
The packaging label for Deviation Distilling LLC's Hand Sanitizer non-sterile solution features 80% alcohol antiseptic topical solution. The label specifies the size as One Gallon (128 FL OZ) or 3.785 L. The Deviation Distilling logo and company address in Denver, CO, are visible along with the website www.deviationdistilling.com.*

* 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.