B Braun S8004-5264 - 0.9% Sodium Chloride Injection USP, 100 mL Fill in 150 mL PAB Container, 64 EA/CA

B Braun S8004-5264 - 0.9% Sodium Chloride Injection USP, 100 mL Fill in 150 mL PAB Container, 64 EA/CA

B Braun S8004-5264 0.9% Sodium Chloride Injection USP, 100 mL Fill in 150 mL PAB Container

Sodium Chloride Injections USP are sterile, nonpyrogenic, isotonic and contain no bacteriostatic or antimicrobial agents. These intravenous solutions are indicated for use in adults and pediatric patients as sources of electrolytes and water for hydration.

• Available in: 25 mL, 50 mL, 100 mL
• No overwrap
• Rigid port system
• Tamper-evident caps
• Not made with natural rubber latex, PVC or DEHP.

B. Braun IV containers are biologically inert and are not made with PVC or the plasticizer DEHP. When certain medications, such as diazepam, nitroglycerin, cyclosporine andor paclitaxel, come in contact with PVC, there is potential for sorption of the drug and therefore the release of DHEP into the fluid and/or absorption of the active ingredient with subsequent subtherapeutic dosing.

Each mL of 0.9% Sodium Chloride Injection USP contains:

• Sodium Chloride USP 9 mg; Water for Injection USP qs
• pH adjusted with Hydrochloric Acid NF
• pH: 5.5 (4.57.0)
• Calculated Osmolarity: 310 mOsmol/liter
• Concentration of Electrolytes (mEq/100 mL): Sodium 15.4 Chloride 15.4

The plastic container is a copolymer of ethylene and propylene formulated and developed for parenteral drugs. The copolymer contains no plasticizers and exhibits virtually no leachability. The safety of the plastic container has been confirmed by biological evaluation procedures. The material passes Class VI testing as specified in the U.S. Pharmacopeia for Biological Tests - Plastic Containers. These tests have shown that the container is nontoxic and biologically inert.

The container/solution unit is a closed system and is not dependent upon entry of external air during administration. The container has two ports, one is for the intravenous administration set and the other is a medication addition site. Each is covered by a tamperproof barrier. Refer to the Directions for Use of the container to properly identify the ports.

Indications and Usage

This intravenous solution is indicated for use in adults and pediatric patients as a source of electrolytes and water for hydration. This product is designed for use as a diluent and delivery system for intermittent intravenous administration of compatible drug additives. Consult prescribing information for INDICATIONS AND USAGE of drug additives to be administered in this manner.