Manganese Injection, Solution
Product Images NDC 0409-4091

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Manganese (NDC 0409-4091). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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

Logo (Manganese 01)

FDA Label Image

Principal Display Panel (10 mL Vial Label)

This is a description of a manganese chloride injection in a 1 ml vial. Each mL vial contains 0.36 mg of manganese chloride tetrahydrate and 9 mg of sodium chloride. The solution has a pH of 2.0 and an osmolality of 0.313 mOsmol/mL (calc). The injection is intended for intravenous use after dilution and has a usual dosage of 1 mg/10 mL (0.1 mg/ml). The vial contains no more than 100 meg/L of aluminum. This product is distributed by Hospira, Inc., based in Lake Forest, IL, USA. The lot/expiry code area is also provided.*

FDA Label Image

Principal Display Panel (10 mL Vial Tray)

Manganese Chloride Injection, USP is a sterile, non-pyrogenic solution containing sodium chloride and hydrochloric acid for pH adjustment. Each mL of the solution contains 0.36mg of tetrahydrate manganese chelates, and 9mg of sodium chloride. The solution is distributed by Hospira, Inc. for intravenous use only after dilution. The rest of the text contains gibberish or errors and cannot be evaluated.*

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