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Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride, and Magnesium Chloride: Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx)
Strength:
526 mg/100 mL, 502 mg/100 mL, 368 mg/100 mL, 37 mg/100 mL, 30 mg/100 mL
Brand names:

Patient information: uses, side effects, how to take - Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride, and Magnesium Chloride

INSTRUCTIONS FOR USE

For Information on Risk of Air Embolism – see DOSAGE AND ADMINISTRATION.

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

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

Do not use solution containers in series connections.

Do not remove solution container from its overwrap until immediately before use.

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

TO OPEN

  1. 1. Always inspect the solution container before and after removal from the overwrap.
  2. 2. Place the solution container on a clean, flat surface. Using the pre-cut corner tabs, peel open the overwrap and remove the solution container from the overwrap.
  3. 3. Check the solution container for leaks by squeezing firmly. If leaks are found, discard as sterility may be impaired.
  4. 4. Do not use if the solution is cloudy or a precipitate is present.

TO PREPARE FOR ADMINISTRATION

  1. 1. Immediately before inserting the infusion set, break off BLUE Infusion Port Cap with the arrow pointing away from the solution container.
  2. 2. Use a non-vented infusion set or close the air-inlet on a vented set.
  3. 3. Close the roller clamp of the infusion set.
  4. 4. Hold the base of BLUE Infusion Port, twist and push the spike until the spike is fully inserted. Refer to complete directions accompanying set.
  5. 5. The BLUE infusion port contains a self‐sealing septum that helps prevent leakage after removing the spike. The infusion port is not intended to be spiked more than once.
  6. 6. Suspend solution container from hanger hole.

If supplemental medication is desired, follow directions below.

TO ADD MEDICATION BEFORE SOLUTION ADMINISTRATION

  1. 1. Identify WHITE Injection Port with arrow pointing toward solution container.
  2. 2. Immediately before injecting additives, break off WHITE Injection Port Cap with the arrow pointing toward solution container.
  3. 3. Hold base of WHITE Injection Port.
  4. 4. Insert needle (18 to 23 gauge) through the center of WHITE Injection Port's septum and inject additives.
  5. 5. Mix solution container contents thoroughly. For high density medication such as potassium chloride, squeeze ports while ports are upright and mix thoroughly.

TO ADD MEDICATION DURING SOLUTION ADMINISTRATION

  1. 1. Close the clamp on the set.
  2. 2. Identify WHITE Injection Port with arrow pointing toward solution container.
  3. 3. Immediately before injecting additives, break off WHITE Injection Port cap with the arrow pointing toward solution container.
  4. 4. Hold base of WHITE Injection Port.
  5. 5. Insert needle (18 to 23 gauge) through the center of WHITE Injection Port's septum and inject additives.
  6. 6. Remove container from IV pole and/or turn to an upright position.
  7. 7. Evacuate both ports by squeezing them while container is in the upright position.
  8. 8. Mix solution container contents thoroughly.
  9. 9. Return container to in use position and continue administration.

For Single Use Only. Discard unused portion.

Manufactured for:

Lake Zurich, IL 60047

Made in Germany

451766

www.fresenius-kabi.com/us

Issued: September 2022

About this document

Source: FDA drug labeling via NLM DailyMed · Application number: ANDA 215370 · View the label on DailyMed

Revision date stated in the text: September 2022

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The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride, and Magnesium Chloride

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Drug class Calculi Dissolution Agent, Osmotic Laxative, Potassium Salt
Active ingredients Sodium chloride 526 mg/100 mL, Sodium gluconate 502 mg/100 mL, Sodium acetate 368 mg/100 mL, Potassium chloride 37 mg/100 mL, Magnesium chloride 30 mg/100 mL
Dosage form Injection, solution
Route Intravenous
Marketing status listed in the FDA NDC Directory
Company (applicant) FRESENIUS KABI USA
FDA approval ANDA 215370Abbreviated New Drug Application (ANDA) – generic drug Approved June 29, 2022
Manufacturers 1 labelers list this drug on DailyMed
Packages (NDC)
Package
526 mg/100 mL, 502 mg/100 mL, 368 mg/100 mL, 37 mg/100 mL, 30 mg/100 mL – 500 ml in 1 bag / 20 in 1 case NDC 65219-387-00
526 mg/100 mL, 502 mg/100 mL, 368 mg/100 mL, 37 mg/100 mL, 30 mg/100 mL – 1000 ml in 1 bag / 10 in 1 case NDC 65219-387-02

Source: FDA drug labeling via NLM DailyMed, data as of November 7, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.