Alcohol Free Hand Sanitizer
Product Images NDC 77042-110

3 FDA label images from Guide Energy Solutions 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 Alcohol Free Hand Sanitizer (NDC 77042-110). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Guide Energy Solutions 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.

Product Images & Figures Index

FDA Label Image

7704211001

7704211001
Label for CleanDurance Alcohol Free Hand Sanitizer by Guide Solutions. The label highlights a 128 fl oz (3785 mL) bottle made in the USA. It notes the product as a 4-hour hand sanitizer with a foaming formula that is non-flammable, dye free, and fragrance free. Active ingredient is Benzalkonium Chloride 0.13% as a skin antiseptic.*
FDA Label Image

7704211002

7704211002
Label for Clean Durance Alcohol Free Hand Sanitizer by Guide Energy Solutions LLC, showing active ingredient Benzalkonium Chloride 0.13% as a skin antiseptic. The product comes in a 2 fl oz (59 mL) container, made in the USA. Features include a foaming formula, non-flammable, dye free, fragrance free, and up to 4-hour hand sanitizing. The label also contains Drug Facts with directions and warnings.*
FDA Label Image

7704211016

7704211016
Label for CleanDurance Alcohol Free Hand Sanitizer by Guide Energy Solutions LLC. The product is alcohol free with benzalkonium chloride 0.13% as the active ingredient. The package indicates a 16 fl oz (473 mL) size and highlights a foaming formula that is non-flammable, dye free, and fragrance free. It states the sanitizer kills 99.99% of germs and is made in the USA.*

* 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.