Suez Gel Formula
Product Images NDC 80896-010

3 FDA label images from Suez Water Technologies & Solutions · 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 Suez Gel Formula (NDC 80896-010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Suez Water Technologies & Solutions, 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

Gel 010 (Suez 12oz 4x5 010 01)

Gel 010 (Suez 12oz 4x5 010 01)
SUEZ Gel Formula 70% Alcohol Gel Antiseptic hand sanitizer in a 12 fl oz (355 mL) bottle. The label features the SUEZ logo, product name, and specifies the antiseptic and alcohol content. It is labeled as a product of SUEZ Water Technologies & Solutions.*
FDA Label Image

Gel 010 (Suez 1gal 4x5 010 01)

Gel 010 (Suez 1gal 4x5 010 01)
SUEZ Gel Formula hand sanitizer gel with 70% alcohol antiseptic strength. The label shows the product name, strength, and gel dosage form. It is manufactured by SUEZ Water Technologies & Solutions. The net content is 128 fl oz (1 gallon, 3.7L). The label includes usage instructions and safety warnings in a Drug Facts format.*
FDA Label Image

Gel 010 (Suez Tote 4x6 010 01)

Gel 010 (Suez Tote 4x6 010 01)
The SUEZ Gel Formula hand sanitizer label features the brand name SUEZ and a logo in green and blue. It states 70% alcohol gel antiseptic and a net content of 275 gallons (1,041 liters). The label includes a Drug Facts panel detailing active ingredients, directions, and other information, and lists the manufacturer as Marquix Ltd located in Hennepin, Illinois.*

* 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.