Product Images Sodium Chloride

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Product Label Images

The following 6 images provide visual information about the product associated with Sodium Chloride NDC 65219-466 by Fresenius Kabi Usa, Llc, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Fresenius Kabi Logo - sod1f 0000 01

Fresenius Kabi Logo - sod1f 0000 01

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Sodium Chloride 50 mL Bag Label - sod1f 0000 02

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Sodium Chloride 50 mL Bag Label - sod1f 0000 02

This is a 50 mL intravenous solution of 0.9% Sodium Chloride Injection, USP for single-use only. It is intended for intravenous use and contains electrolytes such as sodium and chloride. The solution must be discarded after use, and additives to the solution should be mixed thoroughly and must be clear before use. The solution is sterile, and its container is made of non-PVC and non-DEHP substances. It is available only on prescription and must be stored at controlled room temperature, protected from freezing. The manufacturer is Fresenius-Kabi, located in Lake Zurich, IL.*

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Sodium Chloride 100 mL Bag Label - sod1f 0000 03

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Sodium Chloride 100 mL Bag Label - sod1f 0000 03

Free Flex® is a sterile Sodium Chloride Injection solution used for intravenous use. It is only for single-use, and any unused portion must be discarded. Incompatible additives can affect the solution if introduced; thus, a pharmacist's consultation is advisable before adding anything. Before storage, it is essential to check that the solution is clear, and the container is not damaged. The typical dosage is as per the package insert. The solution must be kept within 20° to 25°C (68" to 77°F) [see USP Controlled Room Temperature] to protect it from freezing. The container closure was not made with natural rubber latex. It is Non-PVC, Non-DEHP, sterile, and produced in the USA.*

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Sodium Chloride 250 mL Bag Label - sod1f 0000 04

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Sodium Chloride 250 mL Bag Label - sod1f 0000 04

This is a description of a medication called free flex® NDC 65219-470-05 250 mL 0.9% Sodium Chloride Injection, USP. It is used for intravenous use only and each 100 mL contains sodium chloride in water for injection. The medication should be discarded if unused and the solution is not clear. The usual dosage is available in the package insert, and the medication should be stored at room temperature and protected from freezing. The container closure is not made with natural rubber latex, and it does not contain PVC or DEHP. The medication is manufactured in the USA by Fresenius Kabi.*

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Sodium Chloride 500 mL Bag Label - sod1f 0000 05

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Sodium Chloride 500 mL Bag Label - sod1f 0000 05

This is a description of a 200 ml intravenous solution of 0.9% Sodlum Chloride Injectlon, USP. The solution contains 900 mg Sodium Chloride in water for injection with electrolytes per 1,000 mL: Sodium 154 mEq and Chloride 154 mEq. The solution is for single use, and any leftover solution must be discarded. Additives may not be compatible, and users should consult with pharmacists. The recommended usual dosage is included in the package insert. The container is non-PVC, non-DEHP, sterile, and not made with natural rubber latex. The product must be stored at 20° to 25°C and protected from freezing. The manufacturer is Fresenius Kabi, located in Lake Zurich, IL, USA.*

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Sodium Chloride 1000 mL Bag Label - sod1f 0000 06

PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Sodium Chloride 1000 mL Bag Label - sod1f 0000 06

This is a description of a medication called freeflex. It is a 0.9% Sodium Chloride Injection that is intended for intravenous use only and requires a prescription. The medication comes in a 1,000 mL container that contains 900mg of Sodium Chloride per 100 mL. The container is sterile and does not contain natural rubber, PVC or DEHP. Electrolytes per 1,000 mL are also provided, and the solution must be discarded if it is not used entirely after opening. It is essential to consult with a pharmacist when introducing additives to the solution. The usual dosage should be specified in the package insert, and the medication should be protected from freezing and stored at 20° to 25°C (68° to 77°F).*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.