Hand Gel Sanitizer
Product Images NDC 78851-444

6 FDA label images from Allied Pressroom Products · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Hand Gel Sanitizer (NDC 78851-444). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Allied Pressroom Products, 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

105 mL Label Back (Hand Gel 105 mL Isopropyl Alcohol Back)

105 mL Label Back (Hand Gel 105 mL Isopropyl Alcohol   Back)
Drug Facts panel for Hand Gel Sanitizer containing 70% isopropyl alcohol as the active ingredient. The panel lists purpose, use, warnings, directions, storage instructions, inactive ingredients, and contact information for Allied Pressroom Products.*
FDA Label Image

105 mL Label Front (Hand Gel 105 mL Isopropyl Alcohol Front)

105 mL Label Front (Hand Gel 105 mL Isopropyl Alcohol   Front)
Label for Hand Gel Sanitizer by Allied Pressroom Products, featuring 70% alcohol-based sanitizer. The label states the product contains 70% isopropyl alcohol and emollients (glycerin). It includes a CDC statement recommending use of alcohol-based sanitizers with at least 60% alcohol when soap and water are unavailable. The product volume is 105 mL with fields for batch number and expiration date.*
FDA Label Image

120 mL Label (Hand Gel 120 mL Isopropyl Alcohol)

120 mL Label (Hand Gel 120 mL Isopropyl Alcohol)
Drug Facts panel for Hand Gel Sanitizer by Allied Pressroom Products. The label lists isopropyl alcohol 70% v/v as the active ingredient with antiseptic purpose. It includes warnings, directions for use, storage instructions, and inactive ingredients. The front side highlights the product name, 70% alcohol content, and a CDC statement about using alcohol-based sanitizer if soap and water are unavailable. The package size is 120 mL.*
FDA Label Image

240 mL Label (Hand Gel 240 mL Isopropyl Alcohol)

240 mL Label (Hand Gel 240 mL Isopropyl Alcohol)
Drug Facts and usage panel for Hand Gel Sanitizer by Allied Pressroom Products. The active ingredient is 70% isopropyl alcohol, used as an antiseptic. The panel includes warnings, directions, storage instructions, inactive ingredients, and manufacturer contact information. The front panel shows the product name, alcohol concentration, volume (240 mL), and usage advice from the CDC regarding alcohol-based hand sanitizers.*
FDA Label Image

3785 mL Label (Hand Gel 3785 mL Isoproply Alcohol)

3785 mL Label (Hand Gel 3785 mL Isoproply Alcohol)
Drug Facts panel for Hand Gel Sanitizer by Allied Pressroom Products, containing 70% isopropyl alcohol as the active ingredient. The text includes uses as an antiseptic hand sanitizer, warnings about external use, flammability, and avoiding use on young infants and open wounds. Directions advise application on hands until dry and supervision of young children. Storage instructions recommend keeping the product between 15-30°C and avoiding freezing or excessive heat. Also listed are inactive ingredients and contact information for the manufacturer.*
FDA Label Image

946 mL Label (Hand Gel 946 mL Isoproply Alcohol)

946 mL Label (Hand Gel 946 mL Isoproply Alcohol)
Drug Facts panel for Hand Gel Sanitizer by Allied Pressroom Products, featuring 70% isopropyl alcohol as the active ingredient. The panel includes usage instructions, warnings, directions, inactive ingredients, and storage information. The label also emphasizes the product's alcohol concentration and provides contact information for the manufacturer.*

* 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.