Chlorhexidine Gluconate Rinse
Product Images NDC 17856-2002

4 FDA label images from Atlantic Biologicals Corp. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Chlorhexidine Gluconate (NDC 17856-2002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals Corp., 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
Image Description (Xt Logo)
Label showing Chlorhexidine Gluconate 0.12% oral rinse, USP, produced by Xtrium Laboratories. The label prominently displays the product name and strength along with the NDC 0116-2001-16.*
FDA Label Image

Image Description (Digluconate Chlorhexidine Structure)

Image Description (Digluconate Chlorhexidine Structure)
Chemical structure diagrams showing the molecular structures of Chlorhexidine Gluconate. The image displays detailed atom and bond arrangements for the active ingredient.*
FDA Label Image

Image Description (17856 2002 03)

Image Description (17856 2002 03)
Label for Chlorhexidine Gluconate 0.12% Oral Rinse, showing the dosage strength as 0.12% and packaging in 15 mL cups, quantity 72. The label includes storage instructions (20°C to 25°C, with excursions permitted to 15°C to 30°C) and a reorder phone number. Distributed by Atlantic Biologicals Corps.*
FDA Label Image

Image Description (Cup Label 17856 2002 05)

Image Description (Cup Label 17856 2002 05)
Label for Chlorhexidine Gluconate 0.12% oral rinse, delivering 30 mL, distributed by Atlantic Biologicals Corps. The label includes a barcode, indicates prescription use (RX ONLY), and provides manufacturing and expiration details.*

* 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.