Hand Sanitizer
Product Images NDC 75302-731

View Photos of 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 75302-731). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Spray Products Corporation, 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

Blaster Hs Pour Spout (8 Hs Label 4 10 20p)

Blaster Hs Pour Spout (8 Hs Label 4 10 20p)
The text provides information about the DS Containers hand sanitizer. It contains alcohol as an active ingredient and helps reduce bacteria, for use when soap and water are unavailable. The product should be kept out of eyes, ears, and mouth and not used on children under two months or open skin wounds. Supervision is necessary for children under six years old, as it is flammable. The inactive ingredients include glycerin, hydrogen peroxide, and purified water, and the product should be stored between 15-30C. The product is manufactured for The Blaster Corporation in Cleveland, Ohio.*
FDA Label Image

Blaster Hs Pump Spray (8 Hs Spry Label 4 10 20p)

Blaster Hs Pump Spray (8 Hs Spry Label 4 10 20p)
This text is the drug facts and directions for use of a hand sanitizer containing 80% alcohol as an active ingredient. It provides information on how to use it, warnings against inappropriate use, inactive ingredients, contact information of the manufacturer, and necessary precautions while handling the product.*
FDA Label Image

55 Gal Drum (Hand Sanitizer Drum Label)

55 Gal Drum (Hand Sanitizer Drum Label)
This text provides a sample label for Ethyl Alcohol Formulation Consumer Use, specifically for a hand sanitizer. The product claims to contain 80% alcohol and is intended to be used as an antiseptic to help reduce bacteria that can cause disease when soap and water are not available. The label adheres to FDA guidelines and shares drug facts and directions for use, as well as warning against use in children under two months of age and on open skin wounds. The label instructs users to contact a doctor if they experience irritation or rash and provides additional information on storage and inactive ingredients.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.