cures Sodium Chloride Irrigation Baxter Dosage Form: irrigation 0.9% Sodium Chloride Irrigation, USP in ARTHROMATIC Plastic Container Sodium Chloride Irrigation Baxter Description 0.9% Sodium Chloride Irrigation, USP is a sterile nonpyrogenic, isotonic solution in a single dose ARTHROMATIC plastic container for use as an arthroscopic irrigating solution. Each liter contains 9 g Sodium Chloride, USP (NaCl) in Water for Injection. pH 5.5 (4.5 to 7.0). Milliequivalents per liter: Sodium - 154, Chloride - 154. Osmolarity 308 mOsmol/L (calc.). No antimicrobial agent has been added. The ARTHROMATIC plastic container is fabricated from a specially formulated polyvinyl chloride (PL 146 Plastic). The amount of water that can permeate from inside the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the plastic container can leach out certain of its chemical components in very small amounts within the expiration period, e.g., di-2-ethylhexylphthalate (DEHP), up to 5 parts per million. However, the safety of the plastic has been confirmed in tests in animals according to USP biological tests for plastic containers as well as by tissue culture toxicity studies. Sodium Chloride Irrigation Baxter - Clinical Pharmacology 0.9% Sodium Chloride Irrigation, USP is useful as an irrigating fluid for body joints because the solution is isotonic, and provides a transparent fluid medium with optical properties suitable for good visualization of the interior joint surface during endoscopic examination. During arthroscopic surgical procedures, the solution acts as a lavage for removing blood, tissue fragments, and bone fragments. Indications and Usage for Sodium Chloride Irrigation Baxter 0.9% Sodium Chloride Irrigation, USP is indicated for use as an arthroscopic irrigating fluid with endoscopic instruments during arthroscopic procedures requiring distension and irrigation of the knee, shoulder, elbow, or other bone joints. Contraindications None known. Warnings Not for injection. Because fluids used to irrigate joints may be absorbed into the general circulation, solutions containing sodium ion should be used with great care in patients with congestive heart failure, severe renal insufficiency, and in clinical states in which there exists edema with sodium retention. The contents of an opened container should be used promptly to minimize the possibility of bacterial growth or pyrogen formation. Discard the unused portion of irrigating solution since no antimicrobial agent has been added. Precautions Because some of the fluid used to irrigate joints may be absorbed, caution must be exercised in the volume of irrigating fluid used especially with solutions containing the sodium ion in patients receiving corticosteroids or corticotropin. Pediatric Use Safety and effectiveness in pediatric patients have not been established. Do not administer unless the solution is clear and the seal is intact. Adverse Reactions None known. Sodium Chloride Irrigation Baxter Dosage and Administration The volume of solution needed will vary with the nature and duration of the arthroscopic procedure. If desired, warm in overpouch to near body temperature in a water bath or oven heated to not more than 45º C. Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration whenever solution and container permit. How is Sodium Chloride Irrigation Baxter Supplied 0.9% Sodium Chloride Irrigation, USP in ARTHROMATIC Plastic Container is available as follows: 2B7474 1000 mL NDC 0338-0047-24 2B7477 3000 mL NDC 0338-0047-27 2B7479 5000 mL NDC 0338-0047-29 Exposure of pharmaceutical products to heat should be minimized. Avoid excessive heat. It is recommended the product be stored at room temperature (25º C); brief exposure up to 40º C does not adversely affect the product. DIRECTIONS FOR USE Tear overwrap down side at slit and remove solution container. Some opacity of the plastic due to moisture absorption during the sterilization process may be observed. This is normal and does not affect the solution quality or safety. The opacity will diminish gradually. Check for minute leaks by squeezing bag firmly. If leaks are found, discard solution as sterility may be impaired. Use Aseptic Technique. Suspend container using hanger hole. Remove protector from outlet port. Attach irrigation set. Refer to complete directions accompanying set. Baxter Healthcare Corporation Deerfield, IL 60015 USA Printed in USA 07-19-44-646 Rev. August 2004 Baxter, ARTHROMATIC and PL 146 are trademarks of Baxter International Inc. PACKAGE LABEL.PRINCIPLE DISPLAY PANEL 0.9% Sodium Chloride Irrigation USP Container Label NOT FOR INJECTION 5000 mL 2B7479 NDC 0338-0047-29 0.9% SODIUM CHLORIDE Irrigation USP EACH 100 mL CONTAINS 900 mg SODIUM CHLORIDE USP NO ANTIMICROBIAL AGENT HAS BEEN ADDED pH 5.5 (4.5 to 7.0) mEq/L SODIUM 154 CHLORIDE 154 OSMOLARITY 308 mOsmol/L (CALC) STERILE NONPYROGENIC SINGLE DOSE CONTAINER DO NOT USE UNLESS SOLUTION IS CLEAR DISCARD UNUSED PORTION CAUTIONS SQUEEZE AND INSPECT INNER BAG WHICH MAINTAINS PRODUCT STERILITY DISCARD IF LEAKS ARE FOUND RX ONLY STORE UNIT IN MOISTURE BARRIER OVERWRAP AT ROOM TEMPERATURE (25 C) UNTIL READY TO USE AVOID EXCESSIVE HEAT SEE INSERT 0.9% Sodium Chloride NaCl Irrigation USP ARTHROMATIC CONTAINER PL 146 PLASTIC BAXTER HEALTHCARE CORPORATION DEERFIELD IL 60015 USA MADE IN USA BAXTER ARTHROMATIC AND PL 146 ARE TRADEMARKS OF BAXTER INTERNATIONAL INC FOR PRODUCT INFORMATION 1-800-933-0303 0.9% Sodium Chloride Irrigation USP Carton Label 0.9% SODIUM CHLORIDE IRRIGATION, USP ARTHROMATIC CONT 2-5000ML SECONDARY BAR CODE (17) YYMM00 (10) XXXXX PRIMARY BAR CODE (01) 50303380047296 LOT XXXXX EXP XXXXX 2B7479 SODIUM CHLORIDE sodium chloride irrigant Product Information Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0338-0047 Route of Administration IRRIGATION DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (SODIUM CATION and CHLORIDE ION) SODIUM CHLORIDE 900 mg in 100 mL Inactive Ingredients Ingredient Name Strength WATER Packaging # Item Code Package Description 1 NDC:0338-0047-24 1000 mL in 1 BAG 2 NDC:0338-0047-27 3000 mL in 1 BAG 3 NDC:0338-0047-29 5000 mL in 1 BAG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA017867 05/30/1980 Labeler - Baxter Healthcare Corporation (005083209) Establishment Name Address ID/FEI Operations Baxter Healthcare Corporation 059140764 ANALYSIS(0338-0047), LABEL(0338-0047), MANUFACTURE(0338-0047), PACK(0338-0047), STERILIZE(0338-0047) Revised: 02/2014 Baxter Healthcare Corporation Print this page FEATURED: CAR-T Cell Therapy Overview Mechanism of Action KTE-C19 Studies KTE-C19 Cancer Targets Adverse Events Manufacturing Recently Approved Lonhala Magnair Lonhala Magnair (glycopyrrolate) is a long-acting muscarinic antagonist (LAMA) bronchodilator for... 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