Hand Sanitizer
Product Images NDC 74502-052

3 FDA label images from Octochem, Inc. · 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 Hand Sanitizer (NDC 74502-052). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Octochem, 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

5 Gallon Pail

5 Gallon Pail
Label of GETT Hand Sanitizer by OctoChem, Inc., featuring 75% Isopropyl Alcohol topical solution. The label includes drug facts, warnings, directions, and other information, stating the product is proudly made in the USA. Net contents indicate 128 fluid ounces. The label also displays a satisfaction guarantee and recycling information.*
FDA Label Image

55 Gallon Drum

55 Gallon Drum
Drug Facts panel for GETT Hand Sanitizer containing 75% Isopropyl Alcohol topical solution. The label includes antiseptic use, warnings, directions for application, storage instructions, and inactive ingredients (glycerin, hydrogen peroxide, water). It also states the product is made in the USA and provides a toll-free number and website for the manufacturer.*
FDA Label Image

128oz Case Label (Formula 052 Sanitizer)

128oz Case Label (Formula 052 Sanitizer)
Drug Facts panel for GETT Hand Sanitizer showing active ingredient Isopropyl Alcohol 75% v/v as an antiseptic. The panel includes uses, warnings, directions for use, other information such as storage conditions, and inactive ingredients. The label also displays a satisfaction guarantee and recycling symbol, with net contents marked as 128 fluid ounces.*

* 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.