Sodium Chloride Injection, Solution, Concentrate
Product Images NDC 63323-093

3 FDA label images from Fresenius Kabi Usa, Llc · 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 Sodium Chloride (NDC 63323-093). 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.

FDA Label Image

Logo (Sod0m 0003 01)

FDA Label Image

Package Label (PRINCIPAL DISPLAY – 23.4% Sodium Chloride Injection, USP Vial Label)

Package Label (PRINCIPAL DISPLAY – 23.4% Sodium Chloride Injection, USP Vial Label)
Label for Sodium Chloride Injection, USP, 23.4% concentrate solution with strength 120 mEq/30 mL (4 mEq/mL) in a 30 mL single-dose vial. The label specifies it is a sterile, nonpyrogenic, preservative-free concentrate requiring dilution before intravenous use. It is labeled by Fresenius Kabi USA, LLC, with storage instructions and a barcode on the right side.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – 23.4% Sodium Chloride Injection, USP Tray Label)

Package Label (PRINCIPAL DISPLAY – 23.4% Sodium Chloride Injection, USP Tray Label)
Sodium Chloride Injection, USP 120 mEq/30 mL (4 mEq/mL) concentrate label for intravenous use by Fresenius Kabi USA, LLC. The label states '23.4%' and cautions that the product must be diluted for IV use. It includes dosage form as single-dose vials, with quantity 25 x 30 mL. Additional details such as sterility, preservative-free status, storage instructions, and sodium chloride content are visible along with the bar code and NDC number 63323-093.*

* 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.