Antibacterial Hand Sanitizer Gel
Product Images NDC 73796-110

3 FDA label images from Prostock Llc · 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 Antibacterial Hand Sanitizer (NDC 73796-110). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Prostock Llc, 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

Label (Label)

Label (Label)
Drug Facts panel for Antibacterial Hand Sanitizer gel with 62% ethyl alcohol as the active ingredient. The label includes uses, warnings about external use, flammability, and precautions. Directions for application and storage information are provided. Inactive ingredients include carbomer, fragrance, glycerin, propylene glycol, tocopheryl acetate, triethanolamine, and water. The product is distributed by Prostock LLC, Wayne, NJ, and made in China.*
FDA Label Image

Label2 (Label2)

Label2 (Label2)
Drug Facts panel of Antibacterial Hand Sanitizer gel with 62% ethyl alcohol as active ingredient. Displays antiseptic purpose, uses for hand sanitizing, warnings including flammability and external use, directions for use, and other information such as storage and inactive ingredients. Distributed by Prostock LLC.*
FDA Label Image

Label3 (Label3)

Label3 (Label3)
Label for Antibacterial Hand Sanitizer gel, strength 0.62 mL/mL, in a 2 oz (60 mL) container. The label shows front and back panels with branding, Drug Facts including active ingredient Ethyl Alcohol 62% as an antiseptic, uses, warnings, and directions. Distributed by Prostock LLC, made in China.*

* 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.