Fresh Scent Hand Sanitizer
Product Images NDC 29500-9824

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fresh Scent Hand Sanitizer (NDC 29500-9824). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gl 360, 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

Baby Groot 9824-1 (Baby Groot 9824 1)

Drug Facts panels from the FRESH SCENT HAND SANITIZER 1 FL OZ (29 mL) by GL 360, showing active ingredient ethyl alcohol 62.0% as antimicrobial, usage instructions, warnings about flammability and safety, directions for proper hand sanitizing, and a list of inactive ingredients including water, aloe, carbomer, fragrance, glycerin, propylene glycol, triethanolamine, and tocopheryl acetate.*

FDA Label Image

Captain America 9823-1 (Captain America 9823 1)

Drug Facts panels for FRESH SCENT HAND SANITIZER by GL 360. Panel A shows active ingredient Ethyl Alcohol 62% and antimicrobial purpose. Panel B contains warnings about flammability, eye contact, and keeping out of children’s reach. Panel C provides directions for use and lists inactive ingredients such as water, aloe leaf juice, glycerin, and fragrance.*

FDA Label Image

Captain Marvel 9825-1 (Captain Marvel 9825 1)

Drug Facts panels from a FRESH SCENT HAND SANITIZER label by GL 360, showing active ingredient ethyl alcohol 62.0% as an antimicrobial. The panels include warnings about flammability, eye contact, and keeping out of children's reach, directions for use including hand wetting and rubbing until dry, and a list of inactive ingredients such as water and aloe leaf juice.*

* 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.