Cupric Chloride Injection
Product Images NDC 70069-506

View Photos of Packaging, Regulatory Labels, and Product Appearance

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.

Product Images & Figures Index

FDA Label Image

Image (Ea32e1b7 7c91 478e 9a8c 85f035431e19 01)

Image (Ea32e1b7 7c91 478e 9a8c 85f035431e19 01)
This is a description of a pharmaceutical product called Cupric Chloride Injection, which is intended for intravenous use after dilution. Each mL of the solution contains 0.4 mg of Cupric Chloride, dihydrate 1.07 mg, and sodium chloride 9 mg. The product is available in a 10 mL single-dose vial and the usual dosage information can be found in the insert. The manufacturer is Somerset Therapeutics, LLC., based in Somerset, NJ, and the product is made in India. The packaging includes information regarding aluminum content and emphasizes the necessity to discard any unused portion. The text also provides details such as the manufacturing code, lot number, and expiration date.*
FDA Label Image

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

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

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