Chlorhexidine Gluconate Rinse
Product Images NDC 0121-1786

3 FDA label images from Pai Holdings, Llc Dba Pai Pharma · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Chlorhexidine Gluconate (NDC 0121-1786). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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 (Chlorhex 1)

Chemical Structure (Chlorhex 1)
Chemical structure of Chlorhexidine Gluconate, showing the molecular arrangement of Chlorhexidine combined with Gluconic acid. The structure includes phenyl rings with chlorine substituents and multiple amidine groups connected by a hexamethylene chain, alongside the gluconate moiety.*
FDA Label Image

Label For 473 mL Ndc 0121-1786-16 (Chlorhex 2)

Label For 473 mL Ndc 0121-1786-16 (Chlorhex 2)
This text panel is from a CHLORHEXIDINE GLUCONATE Oral Rinse, USP 0.12% (1.2 mg/mL) bottle by PAI Pharma. It includes usage instructions, warnings on side effects like tooth discoloration, directions for use, storage conditions, ingredients list, and child safety information. It also displays the NDC 0121-1786-16 and bottle size of 16 fl oz (473 mL).*
FDA Label Image

Principal Display Panel (15 mL Cup Label)

Principal Display Panel (15 mL Cup Label)
Round label for Chlorhexidine Gluconate Oral Rinse USP, 0.12%, containing 15 mL. The label includes a barcode, states the product is not child-resistant, and is for prescription use only. Manufacturer is Pharmaceutical Associates, Inc., Greenville, SC.*

* 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.