Calcium Chloride Injection, Solution
Product Images NDC 0517-6710

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Calcium Chloride (NDC 0517-6710). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Regent, 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

Container Label (Calcium Chloride Injection Usp 1)

Container Label (Calcium Chloride Injection Usp 1)
Label for Calcium Chloride Injection, USP, 10% strength (1 Gram/10 mL or 100 mg/mL) in a 10 mL single-dose vial. The label indicates it is for intravenous use only, sterile and nonpyrogenic. Manufactured by American Regent, Inc., the label also includes the NDC 0517-6710-01 and barcode.*
FDA Label Image

Carton Labeling (Calcium Chloride Injection Usp 2)

Carton Labeling (Calcium Chloride Injection Usp 2)
Packaging label for Calcium Chloride 10% Injection, USP, available as 1 Gram/10 mL solution (100 mg/mL) representing 27 mg (1.4 mEq) calcium per mL. The label indicates intravenous use only and contains 10 single-dose 10 mL vials. Manufacturer is American Regent, Inc., Shirley, NY.*
FDA Label Image

Serialization Label (Calcium Chloride Injection Usp 3)

Serialization Label (Calcium Chloride Injection Usp 3)
A label for Calcium Chloride injection solution showing lot number 0000, expiration date January 1999, GTIN 00305176710105, and serial number 1000000000013. The label includes a small 2D barcode in the top left corner. No strength or manufacturer details visible beyond this information.*

* 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.