B Braun L8002 - Solution Sod Cl.9% 250mL Non-DEHP/Non-PVC 250mL/Bg, 24 EA/CA

B Braun L8002 – Solution Sod Cl.9% 250mL Non-DEHP/Non-PVC 250mL/Bg, 24 EA/CA

B Braun L8002 0.9% Sodium Chloride Injection USP, 250 mL

Each 100 mL contains: Sodium Chloride USP 0.45 g; Water for Injection USP qs

pH adjusted with HCl NF pH: 5.6 (4.5-7.0); Calc. Osmolarity: 155 mOsmol/liter, hypotonic

Electrolytes (mEq/liter): Na⁺ 77; Cl^– 77

Sterile, nonpyrogenic. Single dose container. Do not use in series connection. For intravenous use only. Use only if solution is clear and container and seals are intact.

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.

• Not made with natural rubber latex, PVC or DEHP.
• Specific Gravity: 1.006

The plastic container is made from a multilayered film specifically developed for parenteral drugs. It contains no plasticizers and exhibits virtually no leachables. The solution contact layer is a rubberized copolymer of ethylene and propylene. 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 is overwrapped to provide protection from the physical environment and to provide an additional moisture barrier when necessary. Addition of medication should be accomplished using complete aseptic technique. The closure system has two ports; the one for the administration set has a tamper evident plastic protector and the other is a medication addition site. Refer to the Directions for Use of the container.

Indications and Usage of B Braun L8002 0.9% Sodium Chloride Injection USP

0.9% Sodium Chloride Injection USP is indicated for extracellular fluid replacement, treatment of metabolic alkalosis in the presence of fluid loss and mild sodium depletion. 0.9% Sodium Chloride Injection USP is also indicated for use as a priming solution in hemodialysis procedures and may be used to initiate and terminate blood transfusions without hemolyzing red blood cells.

Sodium Chloride Injections USP are also indicated as pharmaceutic aids and diluents for the infusion of compatible drug additives. Refer to prescribing information accompanying additive drugs.

Do not remove overwrap until ready for use. After removing the overwrap, check for minute leaks by squeezing container firmly. If leaks are found, discard solution as sterility may be impaired.