Urigel Neutro Antiseptic Hand Sanitizer Cream Gel 80%
Product Images NDC 80924-002

6 FDA label images from Urigel Inc. · 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 Urigel Neutro Antiseptic Hand Sanitizer Cream Gel 80% (NDC 80924-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Urigel 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

Urigel 500ml Cream Gel (500ml Urigel Cream Gel)

Urigel 500ml Cream Gel (500ml Urigel Cream Gel)
The label for URIGEL 80% Hand Sanitizer Cream Gel by URIGEL INC features the brand name URIGEL prominently with claims of antibacterial and antiviral moisturizing properties. It states the product contains 80% medical degree alcohol and is a cream alcohol in lotion form. The package size is 16.90 fl oz (500 ml). The design includes usage instructions, warnings, and ingredients on the back label.*
FDA Label Image

3ml Packet 80% (Packet 3ml Gel Urigel)

3ml Packet 80% (Packet 3ml Gel Urigel)
URIGEL Hand Sanitizer Gel in a 1.0 fl oz (30 g) silver foil packet. The label shows the brand name URIGEL with a blue background, a chemistry flask icon, and states the product type as hand sanitizer gel. The labeler is indicated as KIMJEM LLC.*
FDA Label Image

Urigel 3.75ml Cream Gel (Urigel Cream Gel 1 Gal)

Urigel 3.75ml Cream Gel (Urigel Cream Gel 1 Gal)
Label for URIGEL 80% Hand Sanitizer Cream Gel by URIGEL INC. The label features a blue and green wave design and states the product is a moisturizing cream alcohol lotion with antibacterial and antiviral properties, containing 80% ethyl alcohol. The net content is 126.8 fl oz (3.96 qt) or 3.75 L. The label includes a drug facts panel, usage directions, warnings, inactive ingredients, distributor information, and a barcode.*
FDA Label Image

Urigel 1000ml Cream Gel (Urigel Cream Gel 1 Ltr)

Urigel 1000ml Cream Gel (Urigel Cream Gel 1 Ltr)
Packaging label of URIGEL 80% Hand Sanitizer Cream Gel by URIGEL INC. The label states it contains 80% ethyl alcohol as an antiseptic and describes the product as a moisturizing cream alcohol lotion with antibacterial and antiviral properties. The volume is 33.81 fl oz (1 L). The label includes drug facts and usage directions, manufacturer and distributor information, and warnings about flammability and external use.*
FDA Label Image

Urigel 250ml Cream Gel (Urigel Cream Gel 250ml)

Urigel 250ml Cream Gel (Urigel Cream Gel 250ml)
Drug Facts panel of URIGEL 80% Hand Sanitizer Cream Gel showing active ingredient ethyl alcohol 80% as antiseptic, use for hand washing to decrease bacteria, warnings including flammability and external use only, directions to wet hands and allow to dry, storage instructions, inactive ingredients listed, and contact information for distribution in USA and Mexico. The front label highlights moisturizing cream alcohol lotion with antibacterial and antiviral properties, volume 8.45 fl oz (250 ml).*
FDA Label Image

Urigel 60ml Cream Gel (Urigel Cream Gel 60ml)

Urigel 60ml Cream Gel (Urigel Cream Gel 60ml)
Packaging label for URIGEL 80% Hand Sanitizer Cream Gel by URIGEL INC. The front shows the brand logo with text highlighting it as a cream alcohol lotion with 80% medical grade alcohol, antibacterial, antiviral, and moisturizing. The bottle size is 2.02 fl oz (60 ml). The back includes a detailed Drug Facts panel listing Ethyl Alcohol 80% as the active ingredient, use instructions, warnings, inactive ingredients (glycerin, hydrogen peroxide, water, paraffin, carbopol 940), storage instructions, and distributor information for USA and Mexico.*

* 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.