Mg Dermasan 72 Gel
Product Images NDC 50241-330

View Photos of 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 Mg Dermasan 72 (NDC 50241-330). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Morgan Gallacher Inc. Dba Custom Chemical Formulators 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.

FDA Label Image

Mg Dermasan 72 1 Gallon

Mg Dermasan 72 1 Gallon
MG DermaSan 72 is a 72% alcohol hand sanitizer gel containing isopropyl alcohol in a 1-gallon (3.785 L) bottle. The label advises it is flammable and for external use only. Manufactured by Morgan Gallacher Inc., the label includes product warnings, usage directions, and active ingredient information.*
FDA Label Image

Mg Dermasan 72 4x1 Box

Mg Dermasan 72 4x1 Box
MG DermaSan 72 gel, a 72% Isopropyl Alcohol hand sanitizer labeled for topical use. The label features warnings such as "Danger: Flammable" and directions for use, including keeping out of reach of children and away from fire or flames. The product is manufactured by Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. and comes in a 4x1 gallon package size.*
FDA Label Image

Mg 55g Dermasan 72

Mg 55g Dermasan 72
Label for MG DermaSan 72 72% Alcohol Hand Sanitizer Gel by Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. The label states USDA Category E3 compliant, quick drying formula with emollients, net content of 55 gallons (208.2 L). Displays active ingredient Isopropyl Alcohol 72%, warnings, directions, flammable symbol, and contact information for emergencies.*

* 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.