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Sodium Chloride Injection, Solution, Concentrate
Product Images NDC 63323-090
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 63323-090). 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.
Package Label (PRINCIPAL DISPLAY – 14.6% Sodium Chloride Injection, USP Vial Label)
Label for Sodium Chloride 14.6% Injection, Concentrate, 50 mEq/20 mL (2.5 mEq/mL) in a 20 mL single dose vial. The label states it is prescription only, preservative free, and for intravenous use. The product is manufactured by Fresenius Kabi USA, LLC, Lake Zurich, IL.*
Package Label (PRINCIPAL DISPLAY – 14.6% Sodium Chloride Injection, USP Tray Label)
Label for Sodium Chloride Injection, USP 14.6% concentrate, containing 50 mEq/20 mL (2.5 mEq/mL) in a single-dose vial. It includes usage instructions indicating it must be diluted before intravenous use. The label specifies preservative-free solution, storage conditions, and manufacturer Fresenius Kabi USA, LLC, Lake Zurich, IL.*
Package Label (PRINCIPAL DISPLAY – 14.6% Sodium Chloride Injection, USP Vial Label)
Label for Sodium Chloride Injection, USP 14.6% concentrate, 100 mEq/40 mL (2.5 mEq/mL) in a 40 mL single dose vial by Fresenius Kabi USA, LLC. The label notes it is a concentrate requiring dilution before intravenous use, with storage and usage instructions including preservative-free content and pH range. The product NDC 63323-090 is visible, along with a barcode.*
Package Label (PRINCIPAL DISPLAY – 14.6% Sodium Chloride Injection, USP Tray Label)
Label for Sodium Chloride Injection, USP 14.6% concentrate, 100 mEq/40 mL (2.5 mEq/mL) in single-dose vials. Contains dosing and dilution instructions, preservative-free statement, pH range, and storage conditions. Manufactured by Fresenius Kabi USA, LLC.*
* 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.
