Cupric Chloride Injection
Product Images NDC 70069-506

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Cupric Chloride (NDC 70069-506). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, Llc, 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 (Ea32e1b7 7c91 478e 9a8c 85f035431e19 01)

Label for Cupric Chloride Injection, USP 4 mg/10 mL (0.4 mg/mL) single-dose vial for intravenous use by Somerset Therapeutics, LLC. The label includes active ingredient details, usage instructions referencing dilution, manufacturing information, and a barcode.*

FDA Label Image

Image (Ea32e1b7 7c91 478e 9a8c 85f035431e19 02)

Label for Cupric Chloride Injection, USP 4 mg/10 mL (0.4 mg/mL) in single-dose vials, supplied by Somerset Therapeutics LLC. The label includes dosage information for intravenous use, manufacturer details, NDC 70069-506, and storage instructions. The label design is white with green, black, and blue text and features barcodes and the Somerset Therapeutics logo.*

* 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.