Freeflex Logo (Sod0r 0004 01)
Sodium Chloride Injection, Solution
Product Images NDC 65219-232
10 FDA label images from Fresenius Kabi Usa, Llc · Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 65219-232). 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.
Product Images & Figures Index
Fresenius Kabi Logo (Sod0r 0004 02)
Package Label (PRINCIPAL DISPLAY – 0.45% Sodium Chloride 50 mL Bag Label)
Label of 0.45% Sodium Chloride Injection, USP, 50 mL solution for intravenous use containing 0.225 grams per 50 mL (4.5 mg/mL) sodium chloride. The single-dose container label includes storage conditions, electrolyte content, manufacturer Fresenius Kabi USA, LLC, and indicates the product is sterile and latex-free. Made in Norway.*
Package Label (PRINCIPAL DISPLAY – 0.45% Sodium Chloride 50 mL Case Label)
Label of 0.45% Sodium Chloride Injection, USP in a 50 mL presentation with packaging quantity of 60 units. The label shows the Freeflex brand marking and indicates storage conditions between 20° to 25°C (68° to 77°F). Manufactured for Fresenius Kabi USA, LLC, Lake Zurich, IL, made in Norway. Expiration and lot fields are placeholders, and barcode symbols are included.*
Package Label (PRINCIPAL DISPLAY – 0.45% Sodium Chloride 100 mL Bag Label)
Label of 0.45% Sodium Chloride Injection, USP, 100 mL intravenous solution by Fresenius Kabi USA, LLC. Contains 0.45 grams per 100 mL (4.5 mg/mL) sodium chloride, with electrolyte content and pH range noted. Single-dose container, sterile, non-PVC and non-DEHP. Storage instructions included. Manufactured in Norway.*
Package Label (PRINCIPAL DISPLAY – 0.45% Sodium Chloride 100 mL Case Label)
Label for 0.45% Sodium Chloride Injection, USP, freeflex®, 100 mL vial, pack of 50. Manufactured for Fresenius Kabi USA, LLC, Lake Zurich, Illinois, made in Norway. Storage instructions indicate 20° to 25°C, protect from freezing. The label includes lot, expiry placeholders, barcodes, and the company website.*
Package Label (PRINCIPAL DISPLAY – 0.45% Sodium Chloride 250 mL Bag Label)
Label for freeflex 0.45% Sodium Chloride Injection, USP, 1.125 grams per 250 mL (4.5 mg/mL) solution for intravenous use. The label specifies electrolyte content, storage instructions, and single-dose container use. Manufactured by Fresenius Kabi USA, LLC, Lake Zurich, IL. The product is sterile, non-PVC, and non-DEHP.*
Package Label (PRINCIPAL DISPLAY – 0.45% Sodium Chloride 250 mL Case Label)
Label of 0.45% Sodium Chloride Injection, USP in 250 mL bags, packaged as 30 units. The label shows the product name, strength, and volume, with storage instructions at 20° to 25°C (68° to 77°F) and protection from freezing. Manufactured for Fresenius Kabi USA, LLC, Lake Zurich, IL, made in Germany. Includes a barcode and lot and expiration date fields.*
Package Label (PRINCIPAL DISPLAY – 0.45% Sodium Chloride 500 mL Bag Label)
Sodium chloride 0.45% Injection, USP in a 500 mL intravenous solution by Fresenius Kabi USA, LLC. The label states 2.25 grams of sodium chloride per 500 mL (4.5 mg per mL) and includes detailed electrolyte content, usage instructions, storage conditions, and manufacturer information. The product is single-dose and sterile, with storage temperature guidelines of 20° to 25°C (68° to 77°F).*
Package Label (PRINCIPAL DISPLAY – 0.45% Sodium Chloride 500 mL Case Label)
Label for 0.45% Sodium Chloride Injection, USP, 500 mL vial, packaged in a quantity of 20. The product is labeled freeflex and manufactured for Fresenius Kabi USA, LLC, located in Lake Zurich, Illinois, made in Germany. Storage instructions specify 20° to 25°C, protecting from freezing.*
* 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.
