Coviside Hand Sanitizer Solution
Product Images NDC 76737-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Coviside Hand Sanitizer (NDC 76737-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Creagen 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

2oz Spray Bottle (2 Oz Label)

Drug Facts panel for Coviside Hand Sanitizer Spray containing 75% isopropyl alcohol. The panel includes active ingredient and purpose, use instructions to reduce bacteria, warnings such as flammability and usage precautions, directions for application, other storage information, and a list of inactive ingredients. The label also shows the product logo, volume (2 oz / 59 mL), manufacturer (CreaGen Inc.), and a Made in USA statement.*

FDA Label Image

4 Oz Spray Bottle (4 Oz Label)

Coviside Hand Sanitizer Spray containing 75% isopropyl alcohol, presented in a 4 oz (118 mL) bottle. The label features this antiseptic hand sanitizer by CREAGEN INC., made in the USA. It includes drug facts about its active ingredient, usage instructions, warnings, storage conditions, and inactive ingredients.*

FDA Label Image

2l Plastic Bottle (Coviside 2l Liquid)

This panel contains Drug Facts for Coviside Hand Sanitizer, listing isopropyl alcohol 75% v/v as the active ingredient and antiseptic purpose. It includes usage, warnings, directions, and storage information. The product is for external use only and flammable, advising avoidance of use in children under two months and on open wounds. Inactive ingredients listed are glycerin, hydrogen peroxide, and purified water USP.*

* 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.