Provon Antimicrobial Foam Handwash Solution
Product Images NDC 0116-8500

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Provon Antimicrobial Foam Handwash (NDC 0116-8500). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xttrium Laboratories, 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

Adx Back Df1 (Adx Back Drug Facts 1)

Drug Facts panel for Provon Antimicrobial Foam Handwash with active ingredient Chlorhexidine gluconate 2% solution. It lists uses for healthcare personnel handwash and surgical hand scrub, warnings for external use only, allergy alert regarding severe allergic reactions, and instructions to avoid eye contact and promptly wash with water if contact occurs. Also includes advice to stop use and seek medical help for serious reactions or if irritation persists.*

FDA Label Image

Adx Back Df2 (Adx Back Drug Facts 2)

Drug Facts panel continued for Provon Antimicrobial Foam Handwash (Chlorhexidine Gluconate 2% topical solution) detailing directions for use by healthcare personnel and surgical hand scrub, warnings to keep out of reach of children and avoid excessive heat, a list of inactive ingredients, and a customer service contact number with hours.*

FDA Label Image

Adx Back Pdp (Adx Back Pdp)

Label for Provon Antimicrobial Foam Handwash with 2% Chlorhexidine Gluconate, a topical antiseptic solution. The label indicates a 42 fl oz (1250 mL) size and is distributed by GOJO Industries, Inc. The product is identified as a human OTC drug with active ingredient Chlorhexidine Gluconate 2%. NDC 0116-8500 is not shown on this label, but the label includes other codes and a barcode.*

FDA Label Image

Adx Front (Adx Front)

Drug Facts panel for Provon Antimicrobial Foam Handwash containing Chlorhexidine Gluconate 2% Solution. The label includes active ingredient and purpose, indicated uses for healthcare personnel handwash, warnings including allergy alert and directions for use. Additional information covers inactive ingredients and storage conditions. The label emphasizes external use only and provides guidance on avoiding serious eye injury and allergic reactions.*

FDA Label Image

Ltx Back Df1 (Ltx Back Drug Facts 1)

Drug Facts panel for Provon Antimicrobial Foam Handwash with active ingredient Chlorhexidine Gluconate 2% solution. The panel details its purpose as an antiseptic, lists uses for healthcare personnel handwash, and provides warnings including directions for use, possible allergic reactions, and precautions.*

FDA Label Image

Ltx Back Df2 (Ltx Back Drug Facts 2)

Drug Facts panel continuation for Provon Antimicrobial Foam Handwash (Chlorhexidine Gluconate 2%) providing directions for use by healthcare personnel and surgical hand scrub instructions. It lists inactive ingredients such as citric acid, cocamide DEA, hydroxyethyl cellulose, isopropyl alcohol, and purified water. Contact information for questions or comments with hours is also included.*

FDA Label Image

Ltx Back Pdp (Ltx Back Pdp)

Label for Provon Antimicrobial Foam Handwash with 2% Chlorhexidine Gluconate solution, antiseptic, in a 40.5 fl oz (1200 mL) size. It is distributed by GOJO Industries, Inc., and manufactured by Xttrium Laboratories, Inc. The label includes the NDC 21749-850-93 and references additional drug facts under the peel flap.*

FDA Label Image

Ltx Front (Ltx Front)

Drug Facts panel for Provon Antimicrobial Foam Handwash, Chlorhexidine Gluconate 2% Solution. It includes active ingredient, antiseptic purpose, uses for healthcare personnel handwash to reduce bacteria, warnings about allergy risks and proper use, directions for use, storage instructions, and listing of inactive ingredients.*

* 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.