Antibacterial Liquid
Product Images NDC 68599-5502

3 FDA label images from Mckesson · 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 Antibacterial (NDC 68599-5502). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mckesson, 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

53-23123-8.5 (53 23123 8.5 (2))

53-23123-8.5 (53 23123 8.5 (2))
Drug Facts label for McKesson Foaming Antibacterial Soap with 0.13% Benzethonium Chloride active ingredient. The label includes uses for handwashing to decrease bacteria, warnings for external use, directions for application, storage information, and a list of inactive ingredients. Contact information for questions is provided.*
FDA Label Image

53-23126-1000 (2) (53 23126 1000 (2))

53-23126-1000 (2) (53 23126 1000 (2))
Label for McKesson Foaming Antibacterial Soap, a topical liquid with 0.13% Benzethonium Chloride antiseptic. The label indicates it is a 1000 mL (34 fl oz) refill for McKesson Pump and Automatic Foam Dispensers. It includes usage instructions, warnings, inactive ingredients, and contact information for questions.*
FDA Label Image

53-23127-18 (2) (53 23127 18 (2))

53-23127-18 (2) (53 23127 18 (2))
Drug Facts panel for McKesson Foaming Antibacterial Soap lists Benzethonium Chloride 0.13% as the active ingredient with antiseptic purpose. It includes uses for handwashing to decrease bacteria, warnings against eye use, directions for application, storage instructions, inactive ingredients, and a customer service contact number. The product is distributed by McKesson Medical-Surgical Inc., Richmond, VA.*

* 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.