Label: STERILE WATER- water injection

  • NDC Code(s): 65219-495-01, 65219-495-10, 65219-497-02, 65219-497-20, view more
    65219-499-03, 65219-499-30
  • Packager: Fresenius Kabi USA, LLC
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated November 18, 2025

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

  • SPL UNCLASSIFIED SECTION

    Soluflex Logo

    Sterile Water for Irrigation, USP

    Rx only

  • DESCRIPTION

    Sterile Water for Irrigation, USP is a sterile, hypotonic, nonpyrogenic irrigating fluid or pharmaceutic aid (solvent) entirely composed of Sterile Water for Injection, USP. It is prepared by distillation and contains no antimicrobial or bacteriostatic agents or added buffers.

    The pH is 5.7 (5.0-7.0)

    The flexible plastic container is made from a multilayered film specifically developed for parenteral drugs. It contains no plasticizers. The solution contact layer is a 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.

    Not made with natural rubber latex, PVC or DEHP.

  • CLINICAL PHARMACOLOGY

    Sterile Water for Irrigation is utilized for a variety of clinical indications. Because of its low refractive index (1.3325), water provides excellent visibility during endoscopic urological procedures. It is also utilized as a pharmaceutic aid, as well as in the preparation of enteral nutrient products.

    Water is hypotonic and will cause hemolysis and will be readily absorbed by the tissues during surgical procedures; therefore, its use under such conditions is not recommended.

  • INDICATIONS AND USAGE

    Sterile Water for Irrigation is indicated for use as an irrigating fluid or pharmaceutic aid. Sterile Water may also be used as an adjunct in the preparation of non-intravenously administered nutrient mixtures (see DOSAGE AND ADMINISTRATION).

  • CONTRAINDICATIONS

    Not for injection.

  • WARNINGS

    Sterile Water for Irrigation is hypotonic and will cause hemolysis, and is not recommended for use during surgical procedures.

    After opening container, its contents should be used promptly to minimize the possibility of bacterial growth or pyrogen formation.

    Discard unused portion of irrigating solution since it contains no preservative.

  • PRECAUTIONS

    Use only if solution is clear and container and seal are intact.

  • ADVERSE REACTIONS

    None known.

    To report SUSPECTED ADVERSE REACTIONS, contact Fresenius Kabi USA, LLC at 1-800-551-7176 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

  • OVERDOSAGE

    None known.

  • DOSAGE AND ADMINISTRATION

    Irrigation

    Use as directed by physician.

    This drug product should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

    Nutrient Mixtures

    Sterile Water for Irrigation, USP may be used to prepare non-intravenously administered nutrient mixtures. It contains no electrolytes or other added substances. Refer to preparation instructions of particular mixture to be used. The plastic container may be used for administration of non-intravenous nutrient mixture to the patient as appropriate.

  • HOW SUPPLIED

    Sterile Water for Irrigation, USP is supplied sterile and nonpyrogenic in single dose flexible plastic containers.

    Product Code

    Unit of Sale

    Each

    495010

    NDC 65219-495-10
    Package of 6 bags

    NDC 65219-495-01
    1000 mL fill in a 1500 mL bag

    497020

    NDC 65219-497-20
    Package of 5 bags

    NDC 65219-497-02
    2000 mL fill in a 2000 mL bag

    499030

    NDC 65219-499-30
    Package of 4 bags

    NDC 65219-499-03
    3000 mL fill in a 3000 mL bag

    Exposure of pharmaceutical products to heat should be minimized. Avoid excessive heat. Protect from freezing. Store at 20° to 25°C (68° to 77°F). [see USP Controlled Room Temperature]; however, brief exposure up to 40°C (104°F) does not adversely affect the product.

  • INSTRUCTIONS FOR USE:

    Not for Injection. Not for use with pressurized irrigation systems.

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

    Irrigation solutions should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

    Do not use if the solution is cloudy or precipitate is present.

    Check the solution container for leaks by squeezing firmly. If leaks are found, discard.

    The intact port cap provides visual tamper evidence. Do not use if port cap is prematurely removed. Maintain strict aseptic technique during handling.

    To Add Medication:

    1.
    Identify WHITE Additive Port with arrow pointing toward solution container.
    2.
    Immediately before injecting additives, break off  WHITE Additive Port Cap with the arrow pointing toward solution container.
    3.
    Hold base of WHITE Additive Port.
    4.
    Insert needle (18 – 23 gauge) through the center of the WHITE Additive Port's resealable septum and inject additives.
    5.
    Mix solution container contents thoroughly.
    6.
    WHITE Additive port must be swabbed with disinfection agent before re-puncturing.
    7.
    Check admixture visually for particulate matter.

    Preparation for Administration

    1.
    Immediately before inserting the irrigation set, break off  BLUE Administration Port Cap with the arrow pointing away from the solution container.
    2.
    Use non-vented irrigation set or close the air-inlet on a vented set. Refer to directions for use accompanying the irrigation set.
    3.
    Hold the base of the BLUE Administration Port, twist and push spike until fully inserted.
    4.
    The BLUE Administration Port contains a self-sealing septum that helps prevent leakage after removing the spike. The Administration Port is not intended to be spiked more than once.
    5.
    Suspend solution container from hanger hole.
    6.
    For Single Use Only. Discard unused portion.

    Manufactured for:

    Fresenius Kabi Logo

    Lake Zurich, IL 60047

    Made in Germany
    www.fresenius-kabi.com/us

    451819
    Issued: September 2024

  • PACKAGE LABEL - PRINCIPAL DISPLAY – Sterile Water for Irrigation, USP 1000 mL Bag Label

    soluflex®      NDC 65219-495-01     1000 mL

    STERILE WATER
    FOR IRRIGATION,
    USP

    INDICATIONS: FOR IRRIGATION

    CONTRAINDICATIONS: NOT FOR INJECTION

    ste0a-0002-01.jpg
  • PACKAGE LABEL - PRINCIPAL DISPLAY - Sterile Water for Irrigation, USP 1000 mL Case Label

    NDC 65219-495-10       495010

    Sterile Water for Irrigation,
    USP

    1,000 mL x 6

    STORE AT: 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]
    Avoid excessive heat. Protect from freezing.

    ste0a-0002-02.jpg
  • PACKAGE LABEL - PRINCIPAL DISPLAY – Sterile Water for Irrigation, USP 2000 mL Bag Label

    soluflex®      NDC 65219-497-02     2000 mL

    STERILE WATER
    FOR IRRIGATION,
    USP

    INDICATIONS: FOR IRRIGATION

    CONTRAINDICATIONS: NOT FOR INJECTION

    ste0a-0002-03.jpg
  • PACKAGE LABEL - PRINCIPAL DISPLAY - Sterile Water for Irrigation, USP 2000 mL Case Label

    NDC 65219-497-20       497020

    Sterile Water for Irrigation,
    USP

    2,000 mL x 5

    STORE AT: 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]
    Avoid excessive heat. Protect from freezing.

    ste0a-0002-04.jpg
  • PACKAGE LABEL - PRINCIPAL DISPLAY – Sterile Water for Irrigation, USP 3000 mL Bag Label

    soluflex®      NDC 65219-499-03     3000 mL

    STERILE WATER
    FOR IRRIGATION,
    USP

    INDICATIONS: FOR IRRIGATION

    CONTRAINDICATIONS: NOT FOR INJECTION

    ste0a-0002-05.jpg
  • PACKAGE LABEL - PRINCIPAL DISPLAY - Sterile Water for Irrigation, USP 3000 mL Case Label

    NDC 65219-499-30       499030

    Sterile Water for Irrigation,
    USP

    3,000 mL x 4

    STORE AT: 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]
    Avoid excessive heat. Protect from freezing.

    ste0a-0002-06.jpg
  • INGREDIENTS AND APPEARANCE
    STERILE WATER 
    water injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:65219-495
    Route of AdministrationIRRIGATION
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER1 mL  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65219-495-106 in 1 CASE12/19/2025
    1NDC:65219-495-011000 mL in 1 BAG; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21612312/19/2025
    STERILE WATER 
    water injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:65219-497
    Route of AdministrationIRRIGATION
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER1 mL  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65219-497-205 in 1 CASE12/19/2025
    1NDC:65219-497-022000 mL in 1 BAG; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21612312/19/2025
    STERILE WATER 
    water injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:65219-499
    Route of AdministrationIRRIGATION
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER1 mL  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65219-499-304 in 1 CASE03/03/2025
    1NDC:65219-499-033000 mL in 1 BAG; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21612303/03/2025
    Labeler - Fresenius Kabi USA, LLC (013547657)
    Establishment
    NameAddressID/FEIBusiness Operations
    Fresenius Kabi Deutschland GmbH506719546MANUFACTURE(65219-495, 65219-497, 65219-499) , ANALYSIS(65219-495, 65219-497, 65219-499) , API MANUFACTURE(65219-495, 65219-497, 65219-499)