Antimicrobial Skin Cleanser Liquid
Product Images NDC 21749-106

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Antimicrobial Skin Cleanser (NDC 21749-106). 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

Back Gojo 1

Drug Facts panel for Antimicrobial Skin Cleanser containing Chlorhexidine Gluconate 2% Solution. The panel lists the active ingredient and its antiseptic purpose. It includes uses for healthcare personnel handwash to help reduce bacteria and surgical hand scrub to reduce microorganisms on hands and forearms before surgery or patient care.*

FDA Label Image

Back Gojo 2

Drug Facts warnings panel for Antimicrobial Skin Cleanser Chlorhexidine Gluconate 2% Solution topical liquid. Includes allergy alert about severe allergic reactions and symptoms, cautions against use by those allergic to chlorhexidine gluconate, and warnings to avoid eyes, ears, and mouth, with advice to seek medical help if irritation or ingestion occurs.*

FDA Label Image

Back Gojo 3

Drug Facts panel continuation for Antimicrobial Skin Cleanser, Chlorhexidine Gluconate 2% Solution. It includes usage directions for premature infants, healthcare personnel handwash, and surgical hand scrub. Other information covers storage instructions. Lists inactive ingredients including citric acid, cocamide DEA, hydroxyethylcellulose, isopropyl alcohol, lauramine oxide, and purified water. Provides a contact number for questions or comments.*

FDA Label Image

Fmx (Fmx 1021 Front)

Label for Provon Antimicrobial Skin Cleanser Chlorhexidine Gluconate 2% Solution, a topical antiseptic liquid. The label shows the product name, strength (20 mg/mL), volume (40.5 fl oz / 1.2 L), and distributor Gojo Industries, Inc. It includes an NDC number 21749-106-89 and has a barcode on the left side.*

FDA Label Image

Prov 32 Drug Facts 1 (Prov32 Drug Facts 1)

Drug Facts panel for Antimicrobial Skin Cleanser (Chlorhexidine Gluconate 2% Solution) describing its uses, warnings, allergy alert, directions on use, and storage information. The panel highlights external use only, cautions on allergic reactions, eye contact precautions, and instructions to keep away from children.*

FDA Label Image

Prov32 Drug Facts 2 (Prov32 Drug Facts 2)

Drug Facts panel detailing directions for use, other information, inactive ingredients, and contact information for questions. Directions cover use with care in premature infants and instructions for surgical hand scrub and health care personnel handwash, including product application and rinsing steps. Other information includes storage temperature, and inactive ingredients list several components such as citric acid and cocamide DEA.*

FDA Label Image

Prov32 Pdp (Prov32 Pdp)

Label for Provon Antimicrobial Skin Cleanser containing Chlorhexidine Gluconate 2% Solution. The product is a topical liquid antiseptic distributed by GOJO Industries, Inc. The label includes the NDC 21749-106-32, net contents of 32 fl oz (1 quart/946 mL), and contact information for the manufacturer. A Drug Facts panel identifying the active ingredient and its purpose as antiseptic is partially visible.*

FDA Label Image

Tfx (Tfx 1021 Front)

Label for Antimicrobial Skin Cleanser Chlorhexidine Gluconate 2% Solution, a topical liquid antiseptic. The product is branded as PROVON and distributed by GOJO Industries, Inc. The label shows a volume of 40.5 fl oz (1.2 L) and includes branding and contact information for GOJO Industries.*

* 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.