Antiseptic Foam Handwash Liquid
Product Images NDC 21749-461

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Antiseptic Foam Handwash (NDC 21749-461). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gojo Industries, 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

Pdp (Gojo Can Pdp)

The packaging label for Provon Antiseptic Lotion Soap with 2% Chlorhexidine Gluconate (CHG) displays the product name and strength. The label indicates it is an antiseptic lotion soap in liquid form, distributed by GOJO Industries, Inc. The volume is 1200 mL (40.5 US/EU FL OZ). Additional details include bar code, manufacturing information, and contact data for GOJO Industries.*

FDA Label Image

Page 1 (Gojo Can Page 1)

Label for PROVON Antiseptic Lotion Soap with 2% Chlorhexidine Gluconate (CHG) by GOJO Industries, Inc. The label includes product use as a general-purpose antimicrobial handwash and directions for use, emphasizing wetting hands, applying soap, working into a lather for 15-30 seconds, rinsing, and drying. Contact information for GOJO Industries in Akron, OH, and GOJO Canada is provided, along with reorder number 5306-04-CAN00.*

FDA Label Image

Page 2 (Gojo Can Page 2)

Drug facts text panel for Antiseptic Foam Handwash with Chlorhexidine Gluconate 2% w/w. It includes active and inactive ingredients, warnings for external use and eye contact, instructions to discontinue use if irritation persists, and keeping out of children's reach. The text is presented in English and French with directions for use and safety precautions.*

* 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.