Structural Formula (Cal09 0001 01)
Calcium Gluconate Injection, Solution
Product Images NDC 65219-164
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 65219-164). 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.
Fresenius Kabi Logo (Cal09 0001 02)
Package Label (PRINCIPAL DISPLAY – Calcium Gluconate 1 g Bag Label)
This is a description of a medication called Calcium Gluconate in Sodium Chloride Injection, used for intravenous administration. It contains 20mg of calcium gluconate per milliliter, totaling 1000mg per vial. The medication should not be diluted, and should not be mixed with other medications. Each milliliter also contains 6.75mg of sodium chloride. The medication comes in a single-dose container and should be discarded if any unused portion remains. The usual dosage is specified in the package insert. The medication should be stored in controlled room temperature between 20° to 25°C (68° to 77°F) and has a total elemental calcium of 93mg (4.65 mEq). The manufacturer is Fresenius Kabi and the medication is made in Norway. There are various lot and expiration numbers specified.*
Package Label (PRINCIPAL DISPLAY – Calcium Gluconate 2 g Bag Label)
This is a description of a medication called Calcium Gluconate, which is dissolved in a solution of Sodium Chloride Injection. It is intended for intravenous use only and comes in a single-dose bag. The bag contains 2,000 mg of Calcium Gluconate per 100 mL of solution. It is not recommended to add an additional medication to the solution. The bag must be discarded after use, and the recommended storage temperature is between 20°C to 25° C. The container closure is not made with natural rubber latex, and it is sterile, non-PVC, and non-DEHP. The manufacturer is Fresenius Kabi, and the medication is made in Norway. The lot number is 0000000, and there is an expiration date indicated as MM-YYYY. There are additional identifying numbers specified as FUM 0441 01-69-03-002A and 403743A.*
* 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.
