Chlorhexidine Gluconate Rinse
Product Images NDC 0116-2001

Product Visual Gallery

This gallery contains 19 technical images submitted to the FDA as part of the official labeling for Chlorhexidine Gluconate (NDC 0116-2001). 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

Xt Logo.jpg (Xt Logo)

Label for Chlorhexidine Gluconate 0.12% Oral Rinse, USP by Xttrium Laboratories, Inc. The label shows the product name, strength (0.12%), and oral rinse dosage form. The labeler logo and NDC base number 0116-2001 are also visible.*

FDA Label Image

1 (Digluconate Chlorhexidine Structure)

Chemical structure diagram of Chlorhexidine Gluconate showing its molecular components and arrangement as represented in the product data for the oral rinse dosage form by Xttrium Laboratories.*

FDA Label Image

16-oz Pdp (Pet16 P)

Packaging label for Chlorhexidine Gluconate Oral Rinse USP 0.12%, a 473 ml (1 pint) oral rinse solution by Xttrium Laboratories, Inc. The label includes directions for use, ingredient listing, and a chemical structure diagram. It states the product is Rx only and highlights safe handling instructions including keeping out of reach of children.*

FDA Label Image

16-oz 1 (Pet16 1)

Text panel displaying clinical pharmacology, pharmacokinetics, indications, contraindications, warnings, precautions, pregnancy and nursing information, pediatric use, and carcinogenesis data for Chlorhexidine Gluconate oral rinse. The text provides detailed safety and efficacy information relevant to healthcare professionals prescribing or dispensing the medication.*

FDA Label Image

Pet 16oz (Xt Oral Rinse Rev Page)

This text panel provides detailed information on Chlorhexidine Gluconate Oral Rinse USP 0.12%, including adverse reactions, overdose warnings, dosage and administration instructions, storage conditions, and how the product is supplied. It also includes chemical structure diagrams of chlorhexidine gluconate and instructions to open the leaflet for further information.*

FDA Label Image

16-oz 3 (Pet16 3)

A drug facts or informational panel titled 'What to Expect When Using Chlorhexidine Gluconate Oral Rinse.' It provides guidance on the use of chlorhexidine gluconate oral rinse, including expected effects like potential taste alteration and teeth/tartar cleaning, warnings about allergic reactions and discoloration, instructions to minimize tooth staining, and advice to contact healthcare providers if there are questions or adverse effects. The text also includes storage temperature recommendations and contact information for reporting side effects.*

FDA Label Image

4-oz Pdp (Pet04 P)

Label for Chlorhexidine Gluconate 0.12% Oral Rinse, USP 4 oz (118 ml) by Xttrium Laboratories, Inc. The label includes directions to swish 1 tablespoon (15 ml) undiluted for 30 seconds, then spit out. It lists active and inactive ingredients and safety instructions, including 'Keep Out of Reach of Children.' The label features the NDC 0116-2001-04 and a barcode.*

FDA Label Image

4-oz 1 (Pet04 1)

Drug facts and prescribing information for Chlorhexidine Gluconate 1.2 mg/mL oral rinse by Xttrium Laboratories, Inc. The text covers description, clinical pharmacology, warnings, contraindications, indications, precautions, and pregnancy and nursing considerations. It details chlorhexidine’s antibacterial activity, use limitations, and dosage notes as an oral rinse.*

FDA Label Image

4-oz 2 (Pet04 2)

Drug facts text panel for Chlorhexidine Gluconate oral rinse 1.2 mg/mL from Xttrium Laboratories. The panel includes overdose instructions, how supplied details with bottle sizes and storage conditions, usage directions, information on what to expect when using the rinse, possible side effects, and a reminder to contact a healthcare provider for advice. It also covers recommended use warnings and provides manufacturer contact information.*

FDA Label Image

Principal Display Panel (Pet15 1)

Label for Chlorhexidine Gluconate 0.12% Oral Rinse, USP, 15 mL bottle, manufactured by Xttrium Laboratories, Inc. The label includes directions for use, ingredients, and a barcode, specifying the product as prescription only and the volume as 0.5 fl oz (15 mL).*

FDA Label Image

15 Oz. Bottle Page 2 (Pet15 2)

This image shows a detailed drug facts and prescribing information panel for Chlorhexidine Gluconate 0.12% Oral Rinse, USP. The text includes a product description, chemical structure, clinical pharmacology, pharmacokinetics, indications and usage, contraindications, and warnings related to this oral rinse product.*

FDA Label Image

15 Oz. Bottle Page 3 (Pet15 3)

Drug facts text panel for Chlorhexidine Gluconate Oral Rinse 1.2 mg/mL by Xttrium Laboratories, Inc. This panel details precautions including effects on gingivitis and tooth staining, taste alterations, and guidance for use during pregnancy, nursing, and pediatric populations. It also addresses carcinogenesis, mutagenesis, and fertility impairment based on animal studies.*

FDA Label Image

15 Oz. Bottle Page 3 (Pet15 4)

Text panel covering adverse reactions, overdose, dosage and administration, supply information, storage conditions, and manufacturer details for Chlorhexidine Gluconate Oral Rinse 1.2 mg/mL by Xttrium Laboratories, Inc. It includes common side effects, instructions for use, packaging description, and safety warnings.*

FDA Label Image

15 Oz. Bottle Page 4 (Pet15 5)

This text panel titled 'What to Expect When Using Chlorhexidine Gluconate Oral Rinse' provides detailed patient information for Chlorhexidine Gluconate 1.2 mg/mL oral rinse by Xttrium Laboratories, Inc. It covers usage directions, warnings about allergic reactions and discoloration, taste effects, instructions to minimize discoloration, storage conditions, ingredient list, and contact information for questions and reporting side effects.*

FDA Label Image

1999xttspdlida (Pet 05)

Unit dose packaging label for Chlorhexidine Gluconate Oral Rinse USP 0.12%, containing 15 mL per dose. The label shows the brand name Chlorhexidine Gluconate, the dosage form as an oral rinse, and the manufacturer Xttrium Laboratories, Inc., located in Mount Prospect, IL. The label includes the NDC 0116-2001-05 and a barcode.*

FDA Label Image

1999chgudcinsta (Insta 1)

Packaging label for Chlorhexidine Gluconate oral rinse 0.12% USP in 15-mL unit dose form. The label includes the proprietary name, dosage form, strength, Rx only designation, and a barcode with the NDC 0116-2001-05. The label is presented in black text on a white background.*

FDA Label Image

1999chgudcinsta (Insta 2)

This panel contains detailed prescribing information for Chlorhexidine Gluconate Oral Rinse USP 0.12%. It includes a product description, clinical pharmacology summary, pharmacokinetics data, indication for use, contraindications, warnings, and precautions. The chemical structure of chlorhexidine gluconate is also depicted.*

FDA Label Image

1999chgudcinsta (Insta 3)

This text panel summarizes adverse reactions, pregnancy and nursing information, pediatric use, carcinogenesis, mutagenesis, impairment of fertility, and other safety precautions related to Chlorhexidine Gluconate oral rinse 1.2 mg/mL. It details possible oral staining, taste alteration, mucosal side effects, and discusses the findings of animal studies relevant to reproductive safety.*

FDA Label Image

1999chgudcinsta (Insta 4)

Drug facts and usage information for Chlorhexidine Gluconate oral rinse, 1.2 mg/mL, including overdose warnings, dosage and administration guidelines, storage instructions, and expected effects. Details cover proper use, potential side effects, and precautions. Labeler information for Xttrium Laboratories, Inc. is also provided.*

* 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.