Hand Sanitizer
Product Images NDC 72655-021

3 FDA label images from Everbrands, Inc. Dba Everpure, Inc. · 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 Hand Sanitizer (NDC 72655-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Everbrands, Inc. Dba Everpure, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

021-04 1oz (021 04 1oz)

021-04 1oz (021 04 1oz)
Drug Facts panel for EverPure Hand Sanitizer, 1 fl. oz., unscented antiseptic. Lists active ingredient, purpose, uses, warnings including flammability and usage instructions, and inactive ingredients (glycerin, hydrogen peroxide, purified water). Includes barcode and manufacturer EverPure information.*
FDA Label Image

021-05 2oz (021 05 2oz)

021-05 2oz (021 05 2oz)
Drug Facts panel for EverPure Hand Sanitizer 2 FL. OZ. The label lists active ingredient as Ethyl Alcohol 62% with the purpose as antiseptic. It includes uses, warnings, directions for use, and inactive ingredients such as glycerin, hydrogen peroxide, and purified water USP. The product is described as unscented and 99.9% effective against most germs.*
FDA Label Image

021-06 4oz (021 06 4oz)

021-06 4oz (021 06 4oz)
Drug Facts panel for Hand Sanitizer by EverPure, Inc. with active ingredient Alcohol 80% v/v as an antiseptic. It includes uses to reduce bacteria, warnings against use in children under 2 months and on open wounds, directions for use, storage instructions, and a list of inactive ingredients. The label also states the product is unscented and antiseptic, with a 4 FL. OZ. volume.*

* 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.