Dmi Cosmetics Wash Me Hand Sanitizer
Product Images NDC 77586-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dmi Cosmetics Wash Me Hand Sanitizer (NDC 77586-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Derma Innovation Company Limited, 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

Image3 (Dmilabel1)

DMI Cosmetics Wash Me Hand Sanitizer packaging labels for 30 ml (1.05 fl. oz) and 50 ml (1.75 fl. oz) bottles. Labels show product name, 75% alcohol content, ingredients, Drug Facts panel including active ingredient Ethyl Alcohol 75%, as well as lot number, manufacturing and expiration dates. Product is labeled as manufactured by DERMA INNOVATION COMPANY LIMITED and a product of Thailand.*

FDA Label Image

Image2 (Dmilabel2)

DMI Cosmetics Wash Me Hand Sanitizer packaging labels featuring 75% alcohol content. The top label is for a 400 ml volume bottle; the bottom label is for a 1 L volume. Both labels include drug facts, active ingredient (ethyl alcohol 75%), warnings, directions, and inactive ingredients. They are labeled as products of Thailand by DERMA INNOVATION COMPANY LIMITED.*

FDA Label Image

Image1 (Dmilabel3)

Label of DMI Cosmetics Wash Me Hand Sanitizer featuring 75% alcohol content. The label includes Drug Facts with active ingredient ethyl alcohol 75% v/v, warnings, directions for use, and inactive ingredients. The product is a 450 ml hand sanitizer gel manufactured by DERMA INNOVATION COMPANY LIMITED and labeled as a product of Thailand.*

* 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.