Structural Formula (Cal0f 0000 01)
Calcium Gluconate Injection, Solution
Product Images NDC 65219-630
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 Calcium Gluconate (NDC 65219-630). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Fresenius Kabi Usa, 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.
Premierprorx Logo (Cal0f 0000 02)
Package Label (PRINCIPAL DISPLAY PANEL)
This is information about a Calcium Gluconate Injection with a concentration of 100 mg per mL in a 10 mL single-dose vial. It is preservative-free and may contain hydrochloric acid or sodium hydroxide for pH adjustment. The solution should not be frozen, and any unused portion should be discarded. It also states that supersaturated solutions are prone to precipitation. The package insert should be consulted for the usual dosage and further details.*
Package Label (PRINCIPAL DISPLAY PANEL)
This text provides information about a sterile injectable solution containing calcium gluconate and calcium saccharate. It includes details on the composition per mL, pH adjustment, osmolality, and aluminum content. The storage instructions, dosage, and precautions for use are also mentioned, emphasizing the importance of checking for clarity and seal integrity before use. The product comes in single-dose vials without preservatives and should be discarded if unused. The text suggests referring to the package insert for further dosage information and warnings about potential precipitation in supersaturated solutions.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
