Hand Gel Sanitizer
Product Images NDC 78851-333

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 78851-333). 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 Back Label (Hand Gel 105 mL Ethyl Alcohol Back)

105 mL Back Label (Hand Gel 105 mL Ethyl Alcohol   Back)
Drug Facts text panel for Hand Gel Sanitizer by Allied Pressroom Products. It lists Ethyl alcohol 70% v/v as the active ingredient with antiseptic purpose, usage instructions, warnings including flammability and age restrictions, directions for use, storage information, and inactive ingredients such as water and glycerin. Contact and company information is included at the bottom.*
FDA Label Image

05 mL Front Label (Hand Gel 105 mL Ethyl Alcohol Front)

05 mL Front Label (Hand Gel 105 mL Ethyl Alcohol   Front)
Label for Hand Gel Sanitizer by Allied Pressroom Products, containing 70% alcohol-based sanitizer with ethyl alcohol and emollients (glycerin). The label includes a CDC statement recommending use of hand sanitizer with at least 60% alcohol when soap and water are unavailable. The product volume is 105 mL with NDC 78851-333-01, and spaces for batch number and expiration date are also present.*
FDA Label Image

120 mL Label (Hand Gel 120 mL Ethyl Alcohol)

120 mL Label (Hand Gel 120 mL Ethyl Alcohol)
Drug Facts panel and product information for Hand Gel Sanitizer by Allied Pressroom Products. The label indicates the hand sanitizer contains 70% ethyl alcohol as the active ingredient and includes warnings, directions, inactive ingredients, and storage instructions. It also states the product size is 120 mL and provides contact details for the labeler.*
FDA Label Image

240 mL Label (Hand Gel 240 mL Ethyl Alcohol)

240 mL Label (Hand Gel 240 mL Ethyl Alcohol)
Drug Facts panel for Hand Gel Sanitizer containing 70% ethyl alcohol as the active antiseptic ingredient. The label includes warnings for external use only, flammability, and precautions against use in children under 2 months and on open wounds. Directions specify applying enough product to cover hands and supervising children under 6 to avoid swallowing. It also lists storage instructions, inactive ingredients, and contact information for Allied Pressroom Products. The right side features the product name, alcohol concentration, usage advice per CDC, NDC code 78851-333-03, and package size of 240 mL.*
FDA Label Image

3785 mL Label (Hand Gel 3785 mL Ethyl Alcohol)

3785 mL Label (Hand Gel 3785 mL Ethyl Alcohol)
Drug Facts panel for Hand Gel Sanitizer by Allied Pressroom Products indicates the active ingredient is 70% v/v ethyl alcohol as an antiseptic. Warnings include flammability and keeping out of reach of children. Directions and other information about usage, storage, and inactive ingredients are provided. The label prominently states 70% alcohol-based sanitizer with expiration and batch number fields.*
FDA Label Image

946 mL Label (Hand Gel 946 mL Ethyl Alcohol)

946 mL Label (Hand Gel 946 mL Ethyl Alcohol)
Drug Facts panel for Hand Gel Sanitizer by Allied Pressroom Products with active ingredient Ethyl alcohol 70% v/v as antiseptic. The panel lists uses, warnings, directions, and other information including flammability, and storage conditions. It emphasizes the use of alcohol-based sanitizers with at least 60% alcohol as stated by the CDC. The product volume is 946 mL and the NDC is 78851-333-04.*

* 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.