Sofresh Hand Sanitizer Ultra Gel
Product Images NDC 78544-101

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sofresh Hand Sanitizer Ultra Gel (NDC 78544-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Qualitary 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

Sofresh Hand Sanitizer Ultra Gel Label 16.9oz

SoFresh Hand Sanitizer Ultra Gel 01 front and back label on a 500 ml bottle. The front highlights 75% alcohol content, kills 99.99% of germs, and contains Aloe & Vitamin E. The back displays detailed Drug Facts including active ingredient Ethyl Alcohol 75% v/v, warnings, directions, inactive ingredients, and distributor information from Qualitary Inc.*

FDA Label Image

Sofresh Hand Sanitizer Ultra Gel Label 33.8oz

SoFresh Hand Sanitizer Ultra Gel 01 front and back label displaying 75% alcohol content with aloe and vitamin E. The front shows the product name, alcohol concentration, and volume (1000 ml). The back label contains Drug Facts, including active ingredient ethyl alcohol 75% v/v and its antimicrobial purpose, usage directions, warnings, inactive ingredients, manufacturer Qualitary Inc, barcode, and contact information.*

FDA Label Image

Sofresh Hand Sanitizer Ultra Gel Label 8oz

SoFresh Hand Sanitizer Ultra Gel 01 75% Alcohol gel in an 8 fl oz (237 ml) bottle. Front label highlights germ-killing efficacy and inclusion of Aloe & Vitamin E. Back label includes Drug Facts with active ingredient Ethyl Alcohol 75% v/v and relevant warnings, usage directions, inactive ingredients, and distributor information from Qualitary Inc.*

* 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.