Calcium Chloride Injection, Solution
Product Images NDC 71872-7045

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Calcium Chloride (NDC 71872-7045). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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.

FDA Label Image

Pdp (7045)

Label for Calcium Chloride Injection, USP 10% (100 mg/mL) in a single-dose syringe. The label indicates intravenous use only, with each mL containing 100 mg calcium chloride dihydrate equivalent to 1.4 mEq Ca++. Manufactured by Hospira, repackaged and distributed by Medical Purchasing Solutions, LLC, Scottsdale, AZ. Includes storage instructions and cautionary statements.*

FDA Label Image

Principal Display Panel (10 mL Syringe Label)

Label for Calcium Chloride 1 g/10 mL (100 mg/mL) injection, USP, packaged in a 10 mL single-dose syringe. The label highlights 10% Calcium Chloride with 1.4 mEq Ca++/mL concentration, for intravenous use only. The product is labeled by Medical Purchasing Solutions, LLC with cautions and storage information.*

FDA Label Image

Logo (Calcium 01a)

FDA Label Image

Principal Display Panel (10 mL Syringe Carton)

Packaging label for Calcium Chloride Injection, USP, 10% strength (1 g/10 mL, 100 mg/mL) in a 10 mL single-dose syringe for intravenous use. The label includes product name, strength, volume, manufacturer Hospira, and directions for aseptic technique use with illustrations. It also notes it is Rx only and features the brand Ansyr™.*

* 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.