Triderma Moisturizing Hand Sanitizer
Product Images NDC 10738-173

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Triderma Moisturizing Hand Sanitizer (NDC 10738-173). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Genuine Virgin Aloe Corporation, 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

8 Fl Oz (0001)

Label for Triderma Moisturizing Hand Sanitizer, an 8 FL OZ (236 mL) no-rinse cleansing gel containing 62% ethyl alcohol. The label highlights moisturizing ingredients aloe, glycerin, and vitamin E. Distributed by Genuine Virgin Aloe Corporation, made in the USA. The label includes drug facts with antimicrobial purpose and usage instructions, warnings, inactive ingredients, and contact information.*

FDA Label Image

2.2 Fl Oz (62 2.2oz Clean 1)

Label of Triderma Moisturizing Hand Sanitizer containing 62% v/v Ethyl Alcohol as the active antimicrobial ingredient. The 2.2 FL OZ (65 mL) bottle is distributed by Genuine Virgin Aloe Corporation. The label highlights moisturizing properties with Aloe and Vitamin E and includes detailed drug facts, warnings, directions, and inactive ingredients information.*

FDA Label Image

4 Fl Oz (62 4oz Clean 1)

Label for Triderma Moisturizing Hand Sanitizer by Genuine Virgin Aloe Corporation featuring 62% ethyl alcohol antimicrobial hand sanitizer. The 4 fl oz (118 mL) formula includes aloe and vitamin E and claims to kill 99.9% of germs. The label also includes Drug Facts with active ingredient, uses, warnings, directions, and inactive ingredients, along with company contact and website information.*

* 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.