Label: SODIUM CHLORIDE injection, solution

  • NDC Code(s): 63323-623-53, 63323-623-61, 63323-623-74, 63323-623-75, view more
  • Packager: Fresenius Kabi USA, LLC
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated April 8, 2021

If you are a consumer or patient please visit this version.


    Rx only


    0.9% Sodium Chloride Injection, USP solution is sterile and nonpyrogenic. It is a parenteral solution containing sodium chloride in water for injection intended for intravenous administration.

    For 0.9% Sodium Chloride Injection, USP, each 100 mL contains 900 mg sodium chloride in water for injection.

    Electrolytes per 1,000 mL: sodium 154 mEq; chloride 154 mEq. The osmolarity is 308 mOsmol/L (calc.).

    The pH in the 100 mL and smaller containers is 6.0; for the 250 mL and larger containers, the pH is 5.6. The pH range is 4.5 to 7.0 for all containers.

    The solution contains no bacteriostat, antimicrobial agent or added buffer and is intended only as a single-dose injection. When smaller doses are required the unused portion should be discarded.

    The solution is a parenteral fluid and electrolyte replenisher.

    Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water.

    Water for injection, USP is chemically designated H2O.

    The flexible container is fabricated from a specially formulated non-plasticized, film containing polypropylene and thermoplastic elastomers (freeflex® bag). The amount of water that can permeate from the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the flexible container can leach out certain of the container's chemical components in very small amounts within the expiration period. The suitability of the container material has been confirmed by tests in animals according to USP biological tests for plastic containers.


    When administered intravenously, the solution provides a source of water and electrolytes.

    Solutions which provide combinations of hypotonic or isotonic concentrations of sodium chloride are suitable for parenteral maintenance or replacement of water and electrolyte requirements.

    Isotonic concentrations of sodium chloride are suitable for parenteral replacement of chloride losses that exceed or equal the sodium loss. Hypotonic concentrations of sodium chloride are suited for parenteral maintenance of water requirements when only small quantities of salt are desired. A hypertonic concentration of sodium chloride may be used to repair severe salt depletion syndrome.

    Sodium chloride in water dissociates to provide sodium (Na+) and chloride (Cl-) ions. Sodium (Na+) is the principal cation of the extracellular fluid and plays a large part in the therapy of fluid and electrolyte disturbances. Chloride (Cl-) has an integral role in buffering action when oxygen and carbon dioxide exchange occurs in the red blood cells. The distribution and excretion of sodium (Na+) and chloride (Cl-) are largely under the control of the kidney which maintains a balance between intake and output.

    Water is an essential constituent of all body tissues and accounts for approximately 70% of total body weight. Average normal adult daily requirements range from two to three liters (1.0 to 1.5 liters each for insensible water loss by perspiration and urine production).

    Water balance is maintained by various regulatory mechanisms. Water distribution depends primarily on the concentration of electrolytes in the body compartments and sodium (Na+) plays a major role in maintaining physiologic equilibrium.


    Intravenous solutions containing sodium chloride are indicated for parenteral replenishment of fluid and sodium chloride as required by the clinical condition of the patient.


    None known.


    Sodium Chloride Injection, USP should be used with great care, if at all, in patients with congestive heart failure, severe renal insufficiency and in clinical states in which there exists edema with sodium retention.

    The intravenous administration of Sodium Chloride Injection, USP can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations, overhydration, congested states or pulmonary edema.

    The risk of dilutive states is inversely proportional to the electrolyte concentration of the injections. The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentrations of the injections.

    In patients with diminished renal function, administration of Sodium Chloride Injection, USP may result in sodium retention.



    Do not use plastic containers in series connections. Such use could result in air embolism due to residual air being drawn from the primary container before administration of the fluid from the secondary container is completed.

    Pressurizing intravenous solutions contained in flexible plastic containers to increase flow rates can result in air embolism if the residual air in the container is not fully evacuated prior to administration.

    Use of a vented intravenous administration set with the vent in the open position could result in air embolism. Vented intravenous administration sets with the vent in the open position should not be used with flexible plastic containers.

    Laboratory Tests

    Clinical evaluation and periodic laboratory determinations are necessary to monitor changes in fluid balance, electrolyte concentrations and acid-base balance during prolonged parenteral therapy or whenever the condition of the patient warrants such evaluation.


    Caution must be exercised in the administration of Sodium Chloride Injection, USP to patients receiving corticosteroids or corticotropin.

    Carcinogenesis, Mutagenesis, Impairment of Fertility

    Studies have not been performed with Sodium Chloride Injection, USP to evaluate the potential for carcinogenesis, mutagenesis or impairment of fertility.


    Teratogenic Effects

    Animal reproduction studies have not been conducted with Sodium Chloride Injection, USP. It is also not known whether Sodium Chloride Injection, USP can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Sodium Chloride Injection, USP should be given to a pregnant woman only if clearly needed.

    Labor and Delivery

    Studies have not been conducted to evaluate the effects of Sodium Chloride Injection, USP on labor and delivery. Caution should be exercised when administering this drug during labor and delivery.

    Nursing Mothers

    It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Sodium Chloride Injection, USP is administered to a nursing mother.

    Pediatric Use

    The use of Sodium Chloride Injection, USP in pediatric patients is based on clinical practice.

    Plasma electrolyte concentrations should be closely monitored in the pediatric population as this population may have impaired ability to regulate fluids and electrolytes.

    Geriatric Use

    Clinical studies of Sodium Chloride Injection, USP did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between elderly and younger patients. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or drug therapy.

    This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.

    Do not administer unless solution is clear and container is undamaged. Discard unused portion.


    Reactions which may occur because of the solution or the technique of administration include febrile response, infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection, extravasation and hypervolemia.

    If an adverse reaction does occur, discontinue the infusion, evaluate the patient, institute appropriate therapeutic countermeasures and save the remainder of the fluid for examination if deemed necessary.


    In the event of overhydration or solute overload, re-evaluate the patient and institute appropriate corrective measures (see WARNINGS, PRECAUTIONS, and ADVERSE REACTIONS).


    The dose is dependent upon the age, weight and clinical condition of the patient.

    Additives may be incompatible. Consult with pharmacist, if available. When introducing additives, use aseptic technique, mix thoroughly and do not store.

    Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit (see PRECAUTIONS).


    Check flexible container solution composition, lot number, and expiry date.

    Do not remove solution container from its overwrap until immediately before use.

    Use sterile equipment and aseptic technique.

    To Open

    1. Turn solution container over so that the text is face down. Using the pre-cut corner tabs, peel open the overwrap and remove solution container.
    2. Check the solution container for leaks by squeezing firmly. If leaks are found, or if the seal is not intact, discard the solution.
    3. Do not use if the solution is cloudy or a precipitate is present.

    To Add Medication

    1. Identify WHITE Additive Port with arrow pointing toward container.
    2. Immediately before injecting additives, break off WHITE Additive Port Cap with the arrow pointing toward container.
    3. Hold base of WHITE Additive Port horizontally.
    4. Insert needle horizontally through the center of WHITE Additive Port's septum and inject additives.
    5. Mix container contents thoroughly.

    Preparation for Administration

    1. Immediately before inserting the infusion set, break off BLUE Infusion Port Cap with the arrow pointing away from container.
    2. Use a non-vented infusion set or close the air-inlet on a vented set.
    3. Close the roller clamp of the infusion set.
    4. Hold the base of BLUE Infusion Port.
    5. Insert spike through BLUE Infusion Port by rotating wrist slightly until the spike is inserted.
      NOTE: See full directions accompanying administration set.

    WARNING: Do not use flexible container in series connections.


    0.9% Sodium Chloride Injection, USP is supplied in single-dose flexible plastic containers as follows:

    Product No.NDC
    StrengthFill SizesBag Size
    623153 63323-623-53 0.9% (9 mg/mL) 50 mL 100 mL
    623161 63323-623-61 0.9% (9 mg/mL) 100 mL 100 mL
    623174 63323-623-74 0.9% (9 mg/mL) 250 mL 250 mL
    623175 63323-623-75 0.9% (9 mg/mL) 500 mL 500 mL
    623176 63323-623-76 0.9% (9 mg/mL) 1,000 mL 1,000 mL

    Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Protect from freezing. The container closure is not made with natural rubber latex. Non-PVC, Non-DEHP, Sterile.

    Manufactured for:

    Fresenius Kabi Logo

    Lake Zurich, IL 60047

    Revised: January 2021


    PACKAGE LABEL - PRINCIPAL DISPLAY PANEL - Sodium Chloride 100 mL Bag Label

                        100 mL

    0.9% Sodium Chloride Injection, USP

    For intravenous use.
    Rx only


    sodium chloride injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:63323-623
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63323-623-5350 mL in 1 BAG; Type 0: Not a Combination Product09/19/2017
    2NDC:63323-623-61100 mL in 1 BAG; Type 0: Not a Combination Product09/19/2017
    3NDC:63323-623-74250 mL in 1 BAG; Type 0: Not a Combination Product09/19/2017
    4NDC:63323-623-75500 mL in 1 BAG; Type 0: Not a Combination Product09/19/2017
    5NDC:63323-623-761000 mL in 1 BAG; Type 0: Not a Combination Product09/19/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Labeler - Fresenius Kabi USA, LLC (608775388)
    NameAddressID/FEIBusiness Operations
    Fresenius Kabi Norge AS731170932ANALYSIS(63323-623) , MANUFACTURE(63323-623)
    NameAddressID/FEIBusiness Operations
    Fresenius Kabi Deutschland GmbH506719546ANALYSIS(63323-623) , MANUFACTURE(63323-623)