Antibacterial Gel
Product Images NDC 78157-000

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Antibacterial Gel (NDC 78157-000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Evolve Verde, S.a. De C.v., 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

Label (Label)

Label for Antibacterial Gel Ethyl Alcohol Antiseptic 70% Topical Solution hand sanitizer by Evolve Verde, S.A. de C.V. The label shows product volume as 3.78 liters (1 US gallon) with active ingredient ethyl alcohol 70%. The label includes directions, warnings, inactive ingredients, and GHS classification for flammability and safety precautions. Manufacturer information is listed as Bio Based Solutions, S.A. de C.V.*

FDA Label Image

Label2 (Label2)

Label for Antibacterial Gel by Evolve Verde, S.A. de C.V., an Ethyl Alcohol Antiseptic 70% topical solution hand sanitizer. The label includes drug facts detailing active ingredient, uses, warnings, directions, and other information. The product size is noted as 208,198 mL, with additional manufacturer information for Bio Based Solutions, S.A. de C.V. Contact details and safety classifications are also present.*

FDA Label Image

Label3 (Label3)

Antibacterial Gel Ethyl Alcohol Antiseptic 70% Topical Solution Hand Sanitizer in a non-sterile solution form, with a large volume of 1,040,000 mL (1040 liters). The label shows the product is formulated by Bio Based Solutions, S.A. de C.V. and includes detailed drug facts, warnings, directions, ingredient list, and GHS classification for flammable liquid. The product is designed for antiseptic use containing 70% ethyl alcohol as the active ingredient.*

* 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.