Sodium Chloride Injection, Solution
Product Images NDC 65219-474

11 FDA label images from Fresenius Kabi Usa, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Sodium Chloride (NDC 65219-474). 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

Fresenius Kabi Logo (Sod1f 0001 01)

FDA Label Image

Package Label – Principal Display Panel – Sodium Chloride 50 mL Bag Label (Sod1f 0001 02)

Package Label – Principal Display Panel – Sodium Chloride 50 mL Bag Label (Sod1f 0001 02)
Label for 0.9% Sodium Chloride Injection, USP, 50 mL intravenous solution by Fresenius Kabi USA, LLC. Each 100 mL contains 900 mg sodium chloride with electrolytes totaling 154 mEq sodium and chloride. The label includes storage instructions, usage cautions, and identifies the product as sterile, non-PVC, non-DEHP, with no natural rubber latex closure.*
FDA Label Image

Package Label – Principal Display Panel – Sodium Chloride 50 mL Case Label (Sod1f 0001 03)

Package Label – Principal Display Panel – Sodium Chloride 50 mL Case Label (Sod1f 0001 03)
Label for 0.9% Sodium Chloride Injection, USP, 50 mL vial, pack of 60. The label includes storage instructions to keep at 20° to 25°C (68° to 77°F) and protect from freezing. Manufactured by Fresenius Kabi USA, LLC, Lake Zurich, IL, with their website listed. The label also features a barcode and placeholders for lot and expiration information.*
FDA Label Image

Package Label – Principal Display Panel – Sodium Chloride 100 mL Bag Label (Sod1f 0001 04)

Package Label – Principal Display Panel – Sodium Chloride 100 mL Bag Label (Sod1f 0001 04)
Label for Sodium Chloride Injection, USP 0.9% solution, 100 mL for intravenous use by Fresenius Kabi USA, LLC. The label indicates each 100 mL contains 900 mg sodium chloride, with electrolyte content and solution pH 4.5 to 7.0 noted. Storage instructions include temperature range 20 to 25°C and protection from freezing. The product is sterile and free of PVC, DEHP, and natural rubber latex in the container closure.*
FDA Label Image

Package Label – Principal Display Panel – Sodium Chloride 100 mL Case Label (Sod1f 0001 05)

Package Label – Principal Display Panel – Sodium Chloride 100 mL Case Label (Sod1f 0001 05)
Label for Sodium chloride 0.9% Injection, USP, showing 100 mL x 50 unit package. The label includes storage instructions to keep at 20° to 25°C (68° to 77°F) and protect from freezing. It displays the Fresenius Kabi logo and contact information, with the product made in the USA by Fresenius Kabi USA, LLC in Lake Zurich, IL. Barcode and lot/expiration placeholders are visible.*
FDA Label Image

Package Label – Principal Display Panel – Sodium Chloride 250 mL Bag Label (Sod1f 0001 06)

Package Label – Principal Display Panel – Sodium Chloride 250 mL Bag Label (Sod1f 0001 06)
Label text panel for 0.9% Sodium Chloride Injection, USP 250 mL by Fresenius Kabi USA, LLC. Contains details on sodium chloride concentration (900 mg/100 mL), electrolytes per 1,000 mL, pH range, storage instructions, usage precautions, and container materials. Indicates single-dose use and storage at controlled room temperature.*
FDA Label Image

Package Label – Principal Display Panel – Sodium Chloride 250 mL Case Label (Sod1f 0001 07)

Package Label – Principal Display Panel – Sodium Chloride 250 mL Case Label (Sod1f 0001 07)
Label for 0.9% Sodium Chloride Injection, USP, 250 mL, packaged in a quantity of 30. The label includes storage instructions to keep at 20° to 25°C (68° to 77°F) and to protect the product from freezing. The labeler is Fresenius Kabi USA, LLC, located in Lake Zurich, IL, with the website www.fresenius-kabi.com/us. The label also contains a barcode and spaces for lot and expiration information.*
FDA Label Image

Package Label – Principal Display Panel – Sodium Chloride 500 mL Bag Label (Sod1f 0001 08)

Package Label – Principal Display Panel – Sodium Chloride 500 mL Bag Label (Sod1f 0001 08)
Label for 0.9% Sodium Chloride Injection USP, 9 mg/mL intravenous solution, packaged in a 500 mL container. The label indicates the product is for prescription use only, with each 100 mL containing 900 mg of sodium chloride. Electrolyte content and pH range are listed. Instructions note single dose use, storage temperature (20° to 25°C), and absence of natural rubber latex. The product is manufactured by Fresenius Kabi USA, LLC.*
FDA Label Image

Package Label – Principal Display Panel – Sodium Chloride 500 mL Case Label (Sod1f 0001 09)

Package Label – Principal Display Panel – Sodium Chloride 500 mL Case Label (Sod1f 0001 09)
Label for 0.9% Sodium Chloride Injection, USP, 500 mL vials in a pack of 20, manufactured by Fresenius Kabi USA, LLC. The label shows storage instructions to keep the product at controlled room temperature (20° to 25°C or 68° to 77°F) and protect it from freezing. The label includes barcode, NDC 65219-472-20, lot and expiration date fields, and company contact information.*
FDA Label Image

Package Label – Principal Display Panel – Sodium Chloride 1000 mL Bag Label (Sod1f 0001 10)

Package Label – Principal Display Panel – Sodium Chloride 1000 mL Bag Label (Sod1f 0001 10)
Label for 0.9% Sodium Chloride Injection, USP, intravenous solution, 1000 mL, with 900 mg sodium chloride per 100 mL. Electrolytes per 1000 mL include 154 mEq sodium and chloride. pH range 4.5 to 7.0. Single dose, non-PVC and non-DEHP container by Fresenius Kabi USA, LLC, Lake Zurich, IL.*
FDA Label Image

Package Label – Principal Display Panel – Sodium Chloride 1,000 mL Case Label (Sod1f 0001 11)

Package Label – Principal Display Panel – Sodium Chloride 1,000 mL Case Label (Sod1f 0001 11)
Label for 0.9% Sodium Chloride Injection, USP 1,000 mL x 10 bags by Fresenius Kabi USA, LLC. The label includes storage instructions to keep at 20° to 25°C (68° to 77°F) and protect from freezing. It shows NDC 65219-474-10, a barcode, and manufacturer location in Lake Zurich, IL, USA.*

* 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.