Helix Hand Sanitizer
Product Images NDC 77732-001

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Helix Hand Sanitizer (NDC 77732-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Helix Spirits 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

Drug Facts (Helix Sanitizer Label Back)

Drug Facts panel for Helix Hand Sanitizer lists Ethanol 80% v/v as the active antimicrobial ingredient. It states uses for reducing bacteria topically when soap and water are unavailable. Warnings include external use only, flammability, and keeping out of children's reach. Directions advise applying enough to cover hands and rubbing until dry. Inactive ingredients are purified water, hydrogen peroxide, and glycerin. Manufactured in Iceland.*

FDA Label Image

Front Label (Helix Sanitizer Label Front)

Label for Helix Hand Sanitizer by Helix Spirits LLC, an alcohol-based hand sanitizer containing 80% alcohol in a 500 ml container. The label includes usage directions, warnings, ingredient composition listing ethanol, glycerol, and hydrogen peroxide, and a graphic of a hand with crossed fingers. Manufacturer website and barcode are also present.*

* 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.