Elevated Mountain Hand Sanitizer
Product Images NDC 74273-001

3 FDA label images from Elevated Mountain Distilling Company · 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 Elevated Mountain Hand Sanitizer (NDC 74273-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Elevated Mountain Distilling Company, 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 (Img 8702 1)

Drug Facts (Img 8702 1)
Drug Facts text panel for Elevated Mountain Hand Sanitizer listing active ingredient as Alcohol 80% v/v with antiseptic purpose. It includes uses to reduce bacteria when soap and water are unavailable, warnings about external use only and flammability, directions for use, storage instructions, and inactive ingredients such as glycerin, hydrogen peroxide, and purified water USP.*
FDA Label Image

Front (Img 8702)

Front (Img 8702)
Label for Elevated Mountain Hand Sanitizer Topical Solution, an alcohol antiseptic non-potable solution containing 80% alcohol. The label shows the brand Elevated Mountain Distilling Company, located in Maggie Valley, NC. The product volume is 1 gallon (3,785.41 ml).*
FDA Label Image

A2445127 802a 74be E053 2995a90abfd6

A2445127 802a 74be E053 2995a90abfd6
Label for Elevated Mountain Hand Sanitizer from Elevated Mountain Distilling Company. It is an 80% alcohol antiseptic topical solution in a 1 gallon (3,785.41 ml) container. The label states the product is a non-potable solution for hand rub use and includes manufacturing details and location in Maggie Valley, NC.*

* 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.