Chlorhexidine Gluconate Liquid
Product Images NDC 0116-0101

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Chlorhexidine Gluconate (NDC 0116-0101). 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

Chemical Structure (Chemical Structure)

Chemical structure of Chlorhexidine Gluconate showing the molecular arrangement of the active ingredient. The diagram includes chlorhexidine components linked to gluconate acid groups.*

FDA Label Image

Patt04 Df1 (Patt04 Df1)

Drug facts panel for Chlorhexidine Gluconate 0.12% oral rinse by Xttrium Laboratories, Inc. The label includes chemical structure, clinical pharmacology, pharmacokinetics, indications, contraindications, warnings, precautions, and information about adverse effects and use in professional dental care. It highlights the antimicrobial action, usage guidelines, and safety information.*

FDA Label Image

Patt04 Df2 (Patt04 Df2)

Drug information text panel for Chlorhexidine Gluconate oral liquid by Xttrium Laboratories, Inc., covering warnings and precautions such as pregnancy and nursing considerations, pediatric and carcinogenicity data, adverse reactions including tooth staining, information on overdose, dosage and administration instructions, as well as warnings about side effects and post marketing reports.*

FDA Label Image

Patt04 Df3 (redacted)

A text panel for Chlorhexidine Gluconate oral rinse, detailing dosage instructions (15 ml undiluted), storage conditions, warnings, allergic reaction advice, usage tips to reduce discoloration and tartar, and contact information for questions and side effects reporting. Manufactured for Patterson Dental Supply, Inc.*

FDA Label Image

Patt04 Pdp (redacted)

Label for Patterson Chlorhexidine Gluconate 0.12% Oral Rinse, USP Mint flavor. The product is a 4 oz. (118 mL) liquid oral rinse with directions for use, active ingredient content, and reorder information. The label indicates it is manufactured for Patterson Dental Supply, Inc., with warnings and barcode present.*

FDA Label Image

Patt16 Df1 (redacted)

This image shows the drug facts and usage information for Chlorhexidine Gluconate 0.12 mg/mL oral rinse by Xttrium Laboratories, Inc. It includes sections on carcinogenesis, mutagenesis, adverse reactions, overdose details, dosage, administration instructions, storage conditions, ingredients, opening and closing instructions, and advice on what to expect when using the oral rinse. It warns about side effects, tooth discoloration, and proper use to minimize risks.*

FDA Label Image

Patt16 Df2 (redacted)

Drug facts and detailed prescribing information for Chlorhexidine Gluconate 0.12% Oral Rinse USP Mint flavor. The panel includes the description, chemical structure, clinical pharmacology, indications, contraindications, warnings, precautions, pregnancy category, nursing mothers' guidance, and pediatric use information. It explains the composition, antimicrobial properties, usage instructions, possible side effects, and safety considerations for this prescription oral rinse.*

FDA Label Image

Patt16 Pdp (redacted)

Patterson Chlorhexidine Gluconate 0.12% oral rinse in mint flavor. Liquid dosage form supplied in a 1 Pint (473 mL) container. Directions for use, storage instructions, and warnings are included. Manufactured by Patterson Dental Supply, Inc. The label highlights active ingredient concentration, usage instructions, and precautions for oral rinse administration.*

* 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.