Adventure Hand Sanitizer
Product Images NDC 77371-021

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Adventure Hand Sanitizer (NDC 77371-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nicety 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.

FDA Label Image

Back (Label 4 Back Unscented Sanitizer Ethyl 60 Final Correct Upc)

Drug Facts panel of Adventure Hand Sanitizer by Nicety Solutions LLC shows the active ingredient as Ethyl Alcohol 60% v/v with antimicrobial purpose. It includes warnings for external use only, flammability, eye contact, and irritation cessation advice. Directions instruct thorough hand spraying and rubbing until dry. Inactive ingredients listed include water, propanediol, aloe vera powder, panthenol, and hydroxyethylcellulose. Contact info and manufacturing details are also provided.*

FDA Label Image

Front (Unscented Front All)

Label for Adventure Hand Sanitizer by NICETY SOLUTIONS LLC, showing it as an unscented hand sanitizer product. The label features a graphic of pine trees and topographic lines, indicates a 1.3 fl oz (38mL) volume, and includes icons suggesting odor removal, germ killing, and suitability for on-the-go use.*

* 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.