Hand Sanitizer
Product Images NDC 76999-7056

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 76999-7056). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gdrg2, 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

250 mL Ndc: 76999-7056-3 (Drjo103 Dr Jon 8.5oz Handsant)

The image shows front and back labels for Dr Jon Hand Sanitizer Refreshing Gel with 73% ethyl alcohol, 8.5 FL oz (250 mL) bottle size, distributed by GDRG2, Inc. The front label highlights "Kills More Than 99.9% of Germs." The back label contains Drug Facts including active ingredient, uses, warnings, directions, and other information, along with a barcode and distributor address.*

FDA Label Image

60 mL Ndc: 76999-7094-5 (Drjo105 Dr Jon 2oz Handsant)

Hand Sanitizer Refreshing Gel 2 FL oz (60 mL) with 73% ethyl alcohol by GDRG2, Inc., shown in bottle and label artwork. Front label displays the brand name DR JON, antimicrobial claims, and product volume. Back label includes Drug Facts panel, warnings, directions, inactive ingredients, distributor information, and a barcode.*

FDA Label Image

29 mL Ndc: 76999-7117-6 (Drjo106 Dr Jon 1oz Handsant)

Packaging label images for Dr. Jon Hand Sanitizer Refreshing Gel, containing 1 FL oz (29 mL). The front label highlights it kills more than 99.9% of germs and contains 73% alcohol. The back label includes Drug Facts, usage instructions, warnings, and inactive ingredients. The product is distributed by GDRG2, 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.