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Dextrose Monohydrate and Sodium Chloride: Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx)
Strength:
5 g/100 mL, 0.225 g/100 mL
Drug class:
Active ingredients:

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

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.

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.

About this document

Source: FDA drug labeling via NLM DailyMed · Application number: ANDA 211221 · View the label on DailyMed

Revision date stated in the text: May 2026

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

Drug information for Dextrose Monohydrate and Sodium Chloride

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Drug class Osmotic Laxative
Active ingredients Dextrose monohydrate 5 g/100 mL, Sodium chloride 0.225 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 211221Abbreviated New Drug Application (ANDA) – generic drug Approved September 15, 2020
Therapeutic equivalence (TE) code APCodes starting with A mean the FDA rates the drug therapeutically equivalent to its reference drug (Orange Book).
Manufacturers 5 labelers list this drug on DailyMed
Packages (NDC)
Package
5 g/100 mL, 0.225 g/100 mL – 250 ml in 1 bag / 30 in 1 case NDC 63323-873-15
5 g/100 mL, 0.225 g/100 mL – 500 ml in 1 bag / 20 in 1 case NDC 63323-873-05
5 g/100 mL, 0.225 g/100 mL – 1000 ml in 1 bag / 10 in 1 case NDC 63323-873-01

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.