Backdrop Distilling Hand Sanitizer
Product Images NDC 74289-001

2 FDA label images from Backdrop Distilling · 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 Backdrop Distilling Hand Sanitizer (NDC 74289-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Backdrop Distilling, 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

Front Label (Backdrop Distilling Hand Sanitizer Front Label Jpg)

Front Label (Backdrop Distilling Hand Sanitizer   Front Label Jpg)
Label for Backdrop Distilling Hand Sanitizer featuring the Backdrop Distilling logo and the GoodLife Brewing Company logo. The label states it is an alcohol antiseptic 70% topical solution hand sanitizer, non-sterile, and indicates the product is from Bend, Oregon.*
FDA Label Image

Drug Facts (Backdrop Distilling Hand Sanitizer Back Label Drug Facts Jpg)

Drug Facts (Backdrop Distilling Hand Sanitizer   Back Label Drug Facts Jpg)
Drug Facts label for Backdrop Distilling Hand Sanitizer includes the active ingredient Ethyl Alcohol 70% v/v as an antiseptic. The text covers uses, warnings, directions, and storage instructions. It advises external use only, avoiding use in children under 2 months, and keeping out of eyes, ears, and mouth. Directions advise placing enough product on hands and rubbing until dry, with supervision for children under 6 years. Inactive ingredients listed are glycerin, hydrogen peroxide, and purified water.*

* 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.