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Sodium Chloride, Lactate, Potassium Chloride, Calcium Chloride, and Dextrose Monohydrate: Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx)
Strength:
600 mg/100 mL, 310 mg/100 mL, 30 mg/100 mL, 20 mg/100 mL, 5 g/100 mL

Patient information: uses, side effects, how to take - Sodium Chloride, Lactate, Potassium Chloride, Calcium Chloride, and Dextrose Monohydrate

INSTRUCTIONS FOR USE

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

Do not remove solution container from its overwrap until immediately before use. Use sterile equipment and aseptic technique.

Flexible Plastic Container (free flex ® bag)

To Open

  1. 1. Turn solution container over so that the text is face down. Using the pre-cut corner tabs, peel open the overwrap and remove solution container.
  2. 2. Check the solution container for leaks by squeezing firmly. If leaks are found, or if the seal is not intact, discard the solution.
  3. 3. Do not use if the solution is cloudy or a precipitate is present.

To Add Medication

  1. 1. Identify WHITE Additive Port with arrow pointing toward container.
  2. 2. Immediately before injecting additives, break off WHITE Additive Port Cap with the arrow pointing toward container.
  3. 3. Hold base of WHITE Additive Port horizontally.
  4. 4. Insert needle horizontally through the center of WHITE Additive Port's septum and inject additives.
  5. 5. Mix container contents thoroughly.

Preparation for Administration

  1. 1. Immediately before inserting the infusion set, break off BLUE Infusion Port Cap with the arrow pointing away from 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.
  5. 5.

    Insert spike through BLUE Infusion Port by rotating wrist slightly until the spike is inserted.

    NOTE: See full directions accompanying administration set.

WARNING: Do not use flexible container in series connections.

Manufactured for:

Lake Zurich, Illinois 60047

Made in Norway

451770

www.fresenius-kabi.com/us

Issued: September 2022

About this document

Source: FDA drug labeling via NLM DailyMed · Application number: ANDA 210332 · 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, Lactate, Potassium Chloride, Calcium Chloride, and Dextrose Monohydrate

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Drug class Blood Coagulation Factor, Osmotic Laxative, Phosphate Binder, Potassium Salt
Active ingredients Sodium chloride 600 mg/100 mL, Sodium lactate 310 mg/100 mL, Potassium chloride 30 mg/100 mL, Calcium chloride 20 mg/100 mL, Dextrose monohydrate 5 g/100 mL
Dosage form Injection, solution
Route Intravenous
Marketing status listed in the FDA NDC Directory
Company (applicant) FRESENIUS KABI USA
FDA approval ANDA 210332Abbreviated New Drug Application (ANDA) – generic drug Approved March 28, 2022
Therapeutic equivalence (TE) code APCodes starting with A mean the FDA rates the drug therapeutically equivalent to its reference drug (Orange Book).
Manufacturers 4 labelers list this drug on DailyMed
Packages (NDC)
Package
600 mg/100 mL, 310 mg/100 mL, 30 mg/100 mL, 20 mg/100 mL, 5 g/100 mL – 1000 ml in 1 bag / 10 in 1 case NDC 65219-241-00
600 mg/100 mL, 310 mg/100 mL, 30 mg/100 mL, 20 mg/100 mL, 5 g/100 mL – 500 ml in 1 bag / 20 in 1 case NDC 65219-243-01

Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.