Nexobrid Kit
Product Images NDC 69866-2015

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 Nexobrid (NDC 69866-2015). 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.

FDA Label Image

20 Gram Carton (20gcarton)

20 Gram Carton (20gcarton)
NEXOBRID kit packaging label for topical gel with 8.8% anacaulase-bcdb. The package indicates the product is for topical use only, with a net weight of 22 grams after mixing. Manufactured by Vericel Corporation, the label includes NDC 69866-2002-3, a barcode, storage instructions, and ingredient details. The label outlines the gel and powder components and specifies it is Rx only.*
FDA Label Image

50 Gram Carton (50gcarton)

50 Gram Carton (50gcarton)
NEXOBRID (anacaulase-bcdb) topical gel kit label from Vericel Corporation, featuring 8.8% gel strength and 55 grams net weight after mixing. The carton includes dosage form and storage instructions, NDC barcode, manufacturer details in Cambridge, MA, and ingredient information describing proteolytic enzymes from pineapple stems.*
FDA Label Image

Not For Sale (Nfscarton)

Not For Sale (Nfscarton)
Packaging label for NEXOBRID topical gel 8.8% (anacaulase-bcdb) in a kit form. The label states "For topical use only" with a net weight of 55 grams after mixing. It includes usage instructions, storage conditions, and manufacturer information for Vericel Corporation. The label notes the product is Rx only and not for sale.*

* 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.