Carticel
Product Images NDC 69866-1025

3 FDA label images from Vericel Corporation · 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 Carticel (NDC 69866-1025). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vericel Corporation, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Principal Display Panel (0.4 mL Vial Label)

Principal Display Panel (0.4 mL Vial Label)
Label for CARTICEL by Vericel Corporation, describing the product as Autologous Cultured Chondrocytes. It includes placeholders for Lot Number, Patient ID, and Expiry Date, with a biohazard symbol and the company address in Cambridge, MA. The label indicates 'Rx only' and features a barcode on the left side.*
FDA Label Image

Principal Display Panel (0.4 mL Vial Shipping Label)

Principal Display Panel (0.4 mL Vial Shipping Label)
Label for CARTICEL, an autologous cultured chondrocytes product by Vericel Corporation. The label states it is for autologous use only, contains approximately 12 million cells per vial in 0.4 mL DMEM with 44 mcg/mL gentamicin, and is stored at room temperature. It notes no preservative or US standard of potency. The product is Rx only and includes placeholder fields for patient ID, lot number, and expiry.*
FDA Label Image

Principal Display Panel (0.4 mL Vial Carton Label)

Principal Display Panel (0.4 mL Vial Carton Label)
Label for CARTICEL, an autologous cultured chondrocytes product by Vericel Corporation. It is for autologous use only and includes patient ID and hospital name placeholders. The label states storage instructions, cell count per vial, absence of preservatives, and that it is Rx only. The label includes lot number, expiry date format, and a barcode with NDC 69866-1025.*

* 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.