Label: PALL STERILE CORD BLOOD COLLECTION UNIT- sterile cord blood collection unit solution

  • NDC Code(s): 79403-791-01
  • Packager: Global Life Sciences Solutions USA LLC
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated December 20, 2023

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

  • ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE SOLUTION (CPD)

    Sterile, non-pyrogenic fluid path. Sterilized by steam.

    This product is free of natural rubber latex.

  • Indications and Usage Section

    For collection of up to 210 ml of umbilical cord blood. Use aseptic technique.

    Contents inside overwrap pouch, within the foil envelope, are sterile and acceptable for use in a sterile field if pouch is unopened and undamaged; visual inspection to confirm the integrity of overwrap pouch should be performed.

  • Warnings Section

    Making multiple punctures of the umbilical cord to increase collection volume may increase the risk of contamination.

    Do not irradiate collected cord blood or components.

  • GENERAL PRECAUTIONS

    Do not use if the package is damaged or seal is incomplete. Use only if solution is clear.
    Sealing should be done in a manner that avoids fluid splatter.

    Always dispose of blood-contaminated products in a manner consistent with established BIOHAZARD safety procedures.

  • HOW SUPPLIED

    The Collection Unit inside the overwrap pouch, within the foil envelope, are sterile and acceptable for use in a sterile field if pouch is unopened and undamaged.

  • INFORMATION FOR PATIENTS

    Visit us at www.pall.com/medical

    For Pall customer service, call: 1.800.645.6578

    DonorCare is a registered trademark of ITL Corporation, Canberra, Australia. Produced under license from ThermoGenesis Corp

    1. Ensure DonorCare® Needle Guard (DCNG) is positioned on the tubing between the needle hub and Pinch Clamp. Engage Pinch Clamp. Ensure tethered cap is placed securely on the air vent.
    2. Using aseptic technique, insert needle into umbilical vein, disengage Pinch Clamp to collect cord blood, mixing frequently, according to standard procedures.
    3. Upon completion of collection, engage Pinch Clamp then withdraw needle from umbilical vein. Slide the DCNG midway over the needle hub. While holding the sides of DCNG near front, grasp tubing and pull smoothly, pulling needle into the DCNG until it locks into place. Confirm that needle is locked by listening for the second click as the needle is drawn into the DCNG. Ensure that tubing cannot be pulled through DCNG.
    4. Place the bag on a work surface. While holding the tubing above the bag, open the tethered cap on the air vent. Allow the blood to drain from the tubing into the bag.
    5. When the tubing has been drained, hold tubing vertical and seal tubing directly below the Y-piece with air vent.
    6. Detach and discard needle, DCNG, Pinch Clamp, Air Vent and tubing according to standard procedures.
    7. Determine amount of anticoagulated blood collected. If required, add sedimenting agent to CPD anticoagulated blood through Sample Port using a syringe according to standard procedures.
    8. Mix well. Take care to strip and mix any blood in tubing.
    9. Load bag into centrifuge cup. It is suggested that a means of support is used to prevent bag from collapsing and to reduce wrinkles.
    10. Centrifuge according to standard procedures to obtain mononuclear cell-rich plasma.

  • PRINCIPAL DISPLAY PANEL

    Printed Pouch LabelIFU_FRIFUCase labelBag label

  • INGREDIENTS AND APPEARANCE
    PALL STERILE CORD BLOOD COLLECTION UNIT 
    sterile cord blood collection unit solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:79403-791
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE0.893 g  in 35 mL
    SODIUM CITRATE (UNII: 1Q73Q2JULR) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) SODIUM CITRATE0.921 g  in 35 mL
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID0.114 g  in 35 mL
    SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN) (PHOSPHATE ION - UNII:NK08V8K8HR) SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE0.0078 g  in 35 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 35 g  in 35 mL
    PHOSPHORIC ACID (UNII: E4GA8884NN)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79403-791-0135 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDABN80022203/16/2011
    Labeler - Global Life Sciences Solutions USA LLC (011658242)
    Establishment
    NameAddressID/FEIBusiness Operations
    Haemonetics Manufacturing Inc.078598396manufacture(79403-791)