Calcium Gluconate Injection, Solution
Product Images NDC 0404-9764

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Calcium Gluconate (NDC 0404-9764). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, 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

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Chemical structure of calcium gluconate showing two gluconate ions complexed with a calcium ion and water molecule, as depicted in the image.*

FDA Label Image

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A dosing information table for Calcium Gluconate injection solution detailing initial and subsequent doses by patient population (neonate, pediatric, adult). It includes mg/kg or mg dosing ranges for bolus and continuous infusion, plus infusion rate limits for adults and pediatric patients, and guidance to adjust continuous infusion rate based on serum calcium levels.*

FDA Label Image

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A data table listing two NDC codes for calcium gluconate injection solution. It details the strength as 1,000 mg calcium gluconate per 10 mL (100 mg/mL) in a 10 mL plastic single-dose vial. One entry indicates packaging in a carton of 25 vials; the other is for individual vials without carton packaging.*

FDA Label Image

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Label for Calcium Gluconate Injection, USP, 1,000 mg per 10 mL single-dose vial. The label indicates the product is preservative free and sterile for intravenous use. It includes storage instructions (20 to 25°C) and cautions about solution appearance. Henry Schein, Inc. is listed as the packager with address in Bastian, VA. The NDC number 0404-9764-10 is shown as a barcode and in text format.*

* 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.