Bacti-gone Liquid
Product Images NDC 67224-693

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bacti-gone (NDC 67224-693). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Beta Technology,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

Beta 4oz (Beta 6930 4oz)

Label for Bacti-Gone Gel Antiseptic Handwash by Beta Technology, Inc. The label states it is for industrial and institutional use and contains 4 fluid ounces. Features a map of the U.S. with "BETA TECHNOLOGY" text. The label includes warnings of flammability and advises to keep out of reach of children.*

FDA Label Image

Beta 6gal (Beta 6930 6 Gal.)

Label for Bacti-Gone Gel Antiseptic Handwash by Beta Technology, Inc. The product is indicated for industrial and institutional use only, with net contents of 6 gallons. The label notes it evaporates quickly and leaves hands soft. The Drug Facts panel lists Ethyl Alcohol 60% as the active ingredient and includes warnings about flammability, external use only, and avoidance of eye contact. Directions and other product information are also provided.*

FDA Label Image

Beta 8oz (Beta 6930 8oz)

Bacti-Gone Gel Antiseptic Handwash liquid, 8 fl. oz., by Beta Technology, Inc. Front label states it kills 99.9% of most common germs, evaporates quickly, and leaves hands soft. Includes warnings about flammability and keeping out of reach of children. The back label provides Drug Facts including active ingredient Ethyl Alcohol 60% (antiseptic), directions for use, warnings, inactive ingredients, and contact information for Beta Technology in Houston, TX. Information is in both English and Spanish.*

* 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.