Kabiven Injection, Emulsion
Product Images NDC 63323-712

Product Visual Gallery

This gallery contains 31 technical images submitted to the FDA as part of the official labeling for Kabiven (NDC 63323-712). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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The text describes different parts of a bag, such as an overpouch notch, handle hole, vertical seals, horizontal seal, and various ports (including a white additive port and a blue infusion port). There is also an oxygen absorber and a caution against using the blind port. The text directs the reader to an instructional video at a website called www.KabivenUSA.com.*

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This text provides instructions for handling KABIVEN®, which is a bag that has three chambers. The bag has one white chamber and two clear chambers. Before activating the bag, it is important to inspect it. If the overpouch is opened or damaged, more than one chamber is white, the solution is yellow, or the seals are already broken, the bag must be discarded. To open the bag, remove the overpouch and place the bag on a clean flat surface. Tear off the noteh. located close to the ports and tear open the long sides to access the inner bag. The overpouch and oxygen absorber should be discarded.*

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The text provides instructions for activating and inspecting a bag of contents, with details on how to roll and apply pressure to the bag to ensure the vertical seals are fully broken. It also states how to confirm activation of the bag by checking that both vertical seals have been broken and the entire contents are white. In addition, the text explains how to identify the correct ports on the bag, with the additive port being white with an arrow pointing toward the bag and the infusion port being blue with an arrow pointing away from the bag.*

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This text provides instructions for adding prescribed additives to a bag. It warns to ensure that the additives are compatible. It instructs breaking off the white additive port cap with the arrow pointing towards the bag before injecting the additives. Additives should be injected by inserting a needle horizontally through the center of the additive port's septum. Aseptic technique should be used for subsequent additions, and the membrane of the additive port is sterile at first use. The septum can be pierced up to 10 times with the recommended needle size of 18 to 23 G 1.5 inches (40mm).*

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This is a set of instructions for using a "Spike and Hang Bag" for medical purposes. It advises the user to break off the blue infusion port cap, to use a non-vented infusion set or close the air-inlet on a vented set, to close the roller clamp, to insert the spike through the infusion port by rotating the wrist, to lift and hold the bag with both hands, and to hang the bag by the hole below the handle. It is important to note that the membrane of the infusion port is sterile for the first use only, and the bag is for single use only; any unused portion should be discarded.*

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This is a product label for an injectable emulsion called KABIVEN® that contains amino acids, electrolytes, dextrose, and lipids. The label includes instructions for use, storage recommendations, dosage information, and activation of the bag. The bag should be rolled tightly until both vertical seals break and the entire contents are white before identifying the correct port for additives and infusion. The product is for intravenous use and should be stored between 2°C and 25°C.*

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Kab02 0000 25

KABIVEN® 4 x 1026 mL is an injectable emulsion used intravenously for amino acids, electrolytes, dextrose, and lipid delivery. The emulsion comes in a sterile, single-dose container with no sulfites added for central infusion. The recommended storage is between 5 to 25 degrees Celsius, and it should be protected from freezing. This container should be discarded if mistakenly frozen, and dosage information is available in the prescribing information. The product is manufactured in Uppsala, Sweden, and contact information for ordering is available on the website of the manufacturer, Fresenius Kabi. Batch number and the manufacturing date are denoted on the label.*

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Kab02 0000 26

The given text seems to be a set of instructions on how to use a medical product called Kabiven, manufactured in Uppsla, Sweden. Kabiven is an injectable emulsion used for intravenous use and contains amino acids, electrolytes, dextrose, and lipids. The bag needs to be activated by rolling it tightly from the top towards the ports, and once the vertical seals break, the bag can be inspected and used for infusion. The total calories in the bag are 1510 Keal, and additives and infusion should be directed to the correct port. The text also mentions to inspect the bag before activation, discard it if more than one chamber is white or if seals are broken.*

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Kab02 0000 27

KABIVEN® is an intravenous emulsion used for electrolytes, dextrose, lipid and amino acid supplementation. The product comes in single-dose sterile containers without any sulfite additives. The recommended storage temperature is between 5°C and 25°C. Customers can order the product by contacting the customer service number or visiting the website. The product is manufactured in Uppsala, Sweden. Batch number, manufacture date and use before date are also listed.*

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Kab02 0000 28

This appears to be a description of a medical product called CABIVEN® 2053 mL, made by KABI in Uppsaia, Sweden, for intravenous use. The product contains amino acids, electrolytes, dextrose, and lipid injectable emulsion. It also includes instructions for use and storage, including activation of the bag, identification of the ports for additives and infusion, and warnings to avoid freezing and excessive heat. The text includes numerous typos and errors, but is still understandable.*

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Kab02 0000 29

KABIVEN® is a sterile injectable emulsion containing amino acids, electrolytes, dextrose, and lipids for intravenous use. It is available in 4 packs of 2053mL and is a single-dose container. The product is manufactured in Uppsala, Sweden, and ordering information can be obtained by calling customer service or visiting the website. The product label contains dosage information and storage conditions, which require storage at 5°C to 25°C and avoiding excessive heat and freezing. The batch number, manufacturing date, and expiration date are also listed on the label.*

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This appears to be a set of instructions for using an intravenous bag called "Nanuractured oy" in Sweden. It is a single dose container with dextrose and lipid for intravenous use. The bag also contains several amino acids, electrolytes and purified egg phospholipids. The instructions mention activation of the bag using a specific technique to ensure the contents are white and to be careful not to use the incorrect port. It is important to consult a pharmacist for additive compatibility and to always use aseptic technique.*

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Kab02 0000 31

KABIVEN® is a sterile injectable emulsion, intended to be given intravenously. It contains amino acids, dextrose, electrolytes, and lipids, with no added sulfites. The product comes in single-dose containers with a dosage established by the prescribing information. It is stored between 5°C and 25°C and must be protected from excessive heat and freezing. The product information includes the manufacturing details such as batch number, manufacturing date, and expiry date. Contact customer service for ordering information.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.