Hand Sanitizer
Product Images NDC 75764-916

2 FDA label images from Mccormick & Company, Incorporated · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 75764-916). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mccormick & Company, Incorporated, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

4.5 Gal Pail Hand Sanitizer (17 L 4 5 Gal Pail 7576491663)

4.5 Gal Pail Hand Sanitizer (17 L 4 5 Gal Pail 7576491663)
Label for McCormick & Company's Hand Sanitizer FB7851 with an active ingredient of 80% alcohol by volume. The label includes Drug Facts, warnings about flammability, and directions for use. It specifies a volume of 4.5 gallons and a weight of 32.85 pounds. The product is distributed by McCormick & Co., Inc., Hunt Valley, MD, and contains ethyl alcohol, glycerin, hydrogen peroxide, and purified water. The label also provides storage temperature guidelines and cautions to supervise children under six years of age.*
FDA Label Image

50 Gal Drum Hand Sanitizer (190 L 50 Gal Drum 7576491664)

50 Gal Drum Hand Sanitizer (190 L 50 Gal Drum 7576491664)
Drug Facts label for Hand Sanitizer FB7851 50GLDR, distributed by McCormick & Company, Incorporated. It lists the active ingredient as Alcohol 80% v/v, its antiseptic purpose, directions for use, warnings about flammability and avoiding contact with eyes, and other storage information. The label also notes inactive ingredients and packaging size of 50.00 gallons (365 lbs).*

* 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.