Icg
Product Images NDC 70599-424

View Photos of 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 Icg (NDC 70599-424). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Karl Storz Endoscopy-america, 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

Chemical Structure (Image 01)

FDA Label Image

Principal Display Panel (Kit Carton Label)

Principal Display Panel (Kit Carton Label)
This is a description of an ICG (Indocyanine green) injection set kit with a 25mg/vial for intravenous administration. The kit is produced by Karl Storz-Endoscope and is stored at a specific temperature range. The left and right panels contain additional information regarding the product, and the back panel has instructions for use enclosed. The provided lot code area does not have any print or coating. The communication methods and contact information for Karl Storz-Endoscope are also included on the packaging.*
FDA Label Image

Principal Display Panel (Vial Label)

Principal Display Panel (Vial Label)
This is a product description for the pharmaceutical product Indocyanine Green. It is available as an injection with 25 mg per vial and is intended for intravenous administration for diagnostic purposes. The product has a shelf life of 6 hours after reconstitution, and must be used within that time. It is a prescription-only drug and is distributed by a company called Green Lo. The text also includes a lot number and expiration date, but they are not included in the output.*
FDA Label Image

Principal Display Panel (Sterile Water Vial Label)

Principal Display Panel (Sterile Water Vial Label)
This is a description for a 10 mL single-dose sterile, nonpyrogenic drug that does not contain any added antimicrobial or other substances. It is for diluent use only and is RX only. The NDC number is 0409-4887-17 and it is manufactured by Hospira, Inc. in Lake Forest, IL 60045, USA.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.