Label: BALANCED SALT- sodium chloride, potassium chloride, calcium chloride, magnesium chloride, sodium acetate, and sodium citrate solution

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated February 21, 2022

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

  • DESCRIPTION

    Balanced Salt Solution Sterile Irrigating Solution is a sterile balanced salt solution, each mL containing sodium chloride (NaCl) 0.64%, potassium chloride (KCl) 0.075%, calcium chloride dihydrate (CaCl2·2H2O) 0.048%, magnesium chloride hexahydrate (MgCl2·6H2O) 0.03%, sodium acetate trihydrate (C2H3NaO2·3H2O) 0.39%, sodium citrate dihydrate (C6H5Na3O7·2H2O) 0.17%, sodium hydroxide and/or hydrochloric acid (to adjust pH), and water for injection.

    The pH is approximately 7.0.

    The osmolality is approximately 300 mOsm/Kg.

  • CLINICAL PHARMACOLOGY

    Balanced Salt Solution Sterile Irrigating Solution is an isotonic solution for use in irrigating tissues of the eyes.

  • INDICATIONS AND USAGE

    For use as an extraocular and intraocular irrigating solution during ocular surgical procedure involving perfusion of the eye with an expected maximum duration of less than 60 minutes.

  • WARNINGS

    • NOT FOR INJECTION OR INTRAVENOUS INFUSION.
    • Do not use unless product is clear, seal is intact and container is undamaged.
    • Do not use if product is discolored or contains a precipitate.
    • SINGLE patient use only. The contents of this bottle should not be used in more than one patient.
    • The use of additives with this solution may cause corneal decompensation.
    • This solution contains no preservative, unused contents should be discarded.
  • PRECAUTIONS

    Open under aseptic conditions only.

    Studies suggest that intraocular irrigating solutions which are iso-osmotic with normal aqueous fluids should be used with caution in diabetic patients undergoing vitrectomy since intraoperative lens changes have been observed.

    There have been reports of corneal clouding or edema following ocular surgery in which Balanced Salt Solution Sterile Irrigating Solution was used as an irrigating solution.

  • ADVERSE REACTIONS

    Irrigation or any other trauma may result in corneal swelling or bullous keratopathy.

    Post-operative inflammatory reactions as well as incidents of corneal edema and corneal decompensation have been reported.

  • DOSAGE AND ADMINISTRATION

    The irrigating solution should be used according to standard format for each surgical procedure. Note: Use an administration set with an air-inlet in the plastic spike since the bottle does not contain a separate airway tube. Follow directions of the particular administration set to be used. Remove the plastic cap of the Flip off closure. Clean and disinfect the rubber stopper by using a sterile alcohol wipe. Insert the spike aseptically into the bottle through the target area of the rubber stopper. Allow the fluid to flow and remove air from the tubing before irrigation begins.

  • HOW SUPPLIED

    Balanced Salt Solution Sterile Irrigating Solution is supplied in a glass bottle using a gray butyl stopper and Flip off closure to close it.

     NDC REFSize 
     Balanced Salt Solution Sterile Irrigating Solution  
     0264-2514-10 S2514-10 500 mL

  • STORAGE

    Store at 20–25°C (68–77°F). Excursions permitted to 15–30°C (59–86°F). [See USP Controlled Room Temperature.] Protect from freezing.

  • SPL UNCLASSIFIED SECTION

    Rx Only

    Revised: November 2019

    B. Braun Medical Inc.
    Bethlehem, PA 18018-3524 USA
    1-800-227-2862

    Y36-002-943 LD-661-1

  • PRINCIPAL DISPLAY PANEL - 500 mL Label

    Balanced Salt Solution

    Sterile Irrigating Solution

    REF S2514-10

    NDC 0264-2514-10

    500 mL

    NOT FOR I.V. USE
    SINGLE USE ONLY

    B. Braun Medical Inc.
    Bethlehem, PA 18018-3524 USA
    1-800-227-2862

    Each mL contains: sodium chloride 0.64%, potassium chloride  0.075%,
    calcium chloride •2H2O 0.048%, magnesium chloride •6H2O  0.03%,
    sodium acetate •3H2O 0.39%, sodium citrate •2H2O 0.17%, sodium
    hydroxide and/or hydrochloric acid (to adjust pH), and water for injection.

    pH: approximately 7.0
    Osmolality: approximately 300 mOsm/Kg

    WARNINGS: NOT FOR INJECTION OR INTRAVENOUS INFUSION.
    Do not use unless product is clear, seal is intact, vacuum is present and
    container is undamaged. Do not use if product is discolored or contains
    a precipitate. Discard unused contents. Do not use this container for
    more than one patient. Do no use additives with this product. Tissue
    damage could result if other drugs are added to product.

    See package insert.

    STERILE              SINGLE DOSE UNIT

    Storage:
    Store at 20-25°C (68-77°F). Excursions permitted to 15-30°C (59-86°F).
    [See USP Controlled Room Temperature.]
    Protect from freezing.

    Rx Only

    Y37-002-524 LD-662-1

    S2514-10 Container Label
     

  • INGREDIENTS AND APPEARANCE
    BALANCED SALT 
    sodium chloride, potassium chloride, calcium chloride, magnesium chloride, sodium acetate, and sodium citrate solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0264-2514
    Route of AdministrationIRRIGATION
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE6.4 mg  in 1 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE0.75 mg  in 1 mL
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CHLORIDE0.48 mg  in 1 mL
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CHLORIDE0.3 mg  in 1 mL
    SODIUM ACETATE (UNII: 4550K0SC9B) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM ACETATE3.9 mg  in 1 mL
    SODIUM CITRATE (UNII: 1Q73Q2JULR) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CITRATE1.7 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0264-2514-10500 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product02/03/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA09138702/03/2010
    Labeler - B. Braun Medical Inc. (002397347)