Calcium Chloride Injection, Solution
Product Images NDC 72572-052

4 FDA label images from Civica, Inc. · 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 Chloride (NDC 72572-052). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Civica, 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 1)

FDA Label Image

Civica Carton (Calcium Chloride Injection 2)

Civica Carton (Calcium Chloride Injection 2)
Label for Calcium Chloride Injection, USP 1 Gram/10 mL (100 mg/mL) intravenous solution. The vial is sterile, nonpyrogenic, single-dose, with a 10 mL volume. Manufactured for Civica, Inc. by American Regent, Inc. Includes caution against intramuscular or subcutaneous injection and notes osmolality and pH values.*
FDA Label Image

Serialization Label (Calcium Chloride Injection 3)

Serialization Label (Calcium Chloride Injection 3)
Calcium Chloride 10% Injection, USP 100 mg/mL intravenous solution in a carton for 10 single-dose vials of 10 mL each. The label states 1 Gram/10 mL (100 mg/mL) represents 27 mg (1.4 mEq) Ca++/mL. Manufactured for Civica, Inc., with distribution by American Regent, Inc.*
FDA Label Image

Calcium Chloride Injection 4

Calcium Chloride Injection 4
Batch and expiration information for Calcium Chloride injection solution is shown, including a QR code, lot number 'TEST', expiration date '11 2020', and a GTIN barcode number. No strength or other product details are visible on this label portion.*

* 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.