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


  1. Description
  2. Clinical Pharmacology
  3. Indications And Usage
  4. Warnings
  5. Precautions
  6. Adverse Reactions
  7. Dosage And Administration
  8. How Supplied
  9. Storage
  10. Principal Display Panel - 500 Ml Label

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 aluminum tab. 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 aluminum closure with a tear tab.

NDC REF Size
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.

 

Rx Only

Issued: November 2009

B. Braun Medical Inc.
Irvine, CA 92614-5895 USA
Made in USA

Y36-002-712

Principal Display Panel - 500 Ml Label 

Balanced Salt Solution

Sterile Irrigating Solution

NDC 0264-2514-10
REF S2514-10

500 mL

NOT FOR I.V. USE
SINGLE USE ONLY

B. Braun Medical Inc.
Irvine, CA 92614-5895 USA
Made in USA

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

Y37-002-363

PRINCIPAL DISPLAY PANEL - 500 mL Label
BALANCED SALT
sodium chloride, potassium chloride, calcium chloride, magnesium chloride, sodium acetate, and sodium citrate solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0264-2514
Route of Administration IRRIGATION
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 6.4 mg in 1 mL
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE 0.75 mg in 1 mL
CALCIUM CHLORIDE (UNII: M4I0D6VV5M) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CHLORIDE 0.48 mg in 1 mL
MAGNESIUM CHLORIDE (UNII: 02F3473H9O) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CHLORIDE 0.3 mg in 1 mL
SODIUM ACETATE (UNII: 4550K0SC9B) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM ACETATE 3.9 mg in 1 mL
SODIUM CITRATE (UNII: 1Q73Q2JULR) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CITRATE 1.7 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM HYDROXIDE (UNII: 55X04QC32I)
HYDROCHLORIC ACID (UNII: QTT17582CB)
WATER (UNII: 059QF0KO0R)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0264-2514-10 12 in 1 CASE 02/03/2010
1 500 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA091387 02/03/2010
Labeler - B. Braun Medical Inc. (002397347)

Revised: 12/2018 B. Braun Medical Inc.



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