DEXTROSE AND SODIUM CHLORIDE injection, solution

Dextrose and Sodium Chloride by

Drug Labeling and Warnings

Dextrose and Sodium Chloride by is a Prescription medication manufactured, distributed, or labeled by Baxter Healthcare Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • 1 INDICATIONS AND USAGE

    Dextrose and Sodium Chloride Injection is indicated as a source of water, electrolytes and calories.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Important Administration Instructions

    • Dextrose and Sodium Chloride Injection is only for intravenous infusion.
    • The osmolarity of Dextrose and Sodium Chloride Injection, ranges from 280 to 560 mOsmol/L (calc). Peripheral administration is generally acceptable; however; consider central vein administration if there is peripheral vein irritation, phlebitis, and/or associated pain.
    • Do not administer Dextrose and Sodium Chloride Injection simultaneously with blood products through the same administration set because of the possibility of pseudoagglutination or hemolysis.
    • To prevent air embolism, use a non-vented infusion set or close the vent on a vented set, avoid multiple connections, do not connect flexible containers in series, fully evacuate residual gas in the container prior to administration, do not pressurize the flexible container to increase flow rates, and if administration is controlled by a pumping device, turn off pump before the container runs dry.
    • Prior to infusion, visually inspect the solution for particulate matter. The solution should be clear and there should be no precipitates. Do not administer unless solution is clear and container is undamaged.
    • Use of a final filter is recommended during administration of parenteral solutions, where possible.

    2.2 Recommended Dosage

    The choice of the specific, sodium chloride, and dextrose concentrations, rate and volume depends on the age, weight, clinical and metabolic conditions of the patient and concomitant therapy. Electrolyte supplementation may be indicated according to the clinical needs of the patient.

    The administration rate should be governed, especially for premature infants with low birth weight, during the first few days of therapy, by the patient’s tolerance to dextrose. Increase the infusion rate gradually as indicated by frequent monitoring of blood glucose concentrations [see Warnings and Precautions (5.2), Use in Specific Populations (8.4)].

    2.3 Instructions for Use

    To Open

    • Do not remove container from overwrap until ready to use.
    • Tear overwrap down side at slit and remove solution container.
    • Visually inspect the container. Some opacity of the plastic due to moisture absorption during the sterilization process may be observed. This is normal and does not affect the solution quality or safety. The opacity will diminish gradually. Evaluate the following:
      • ∘ If the outlet port protector is damaged, detached, or not present, discard container.
      • ∘ Check to ensure the solution is clear and there are no precipitates. Discard if there is a color change and/or the appearance of precipitates, insoluble complexes or crystals.
      • ∘ Check for minute leaks by squeezing inner bag firmly. If leaks are found, discard container.

    Preparation for Administration

    • 1. Suspend container from eyelet support.
    • 2. Remove protector from outlet port at bottom of container.
    • 3. Attach administration set. Refer to complete directions accompanying set.

    To Add Medication

    • Additives may be incompatible. Complete information is not available. Do not use additives known or determined to be incompatible.
    • Consult with pharmacist, if available. If, in the informed judgment of the healthcare provider, it is deemed advisable to introduce additives, use aseptic technique.
    • When introducing additives, consult the instructions for use of the medication to be added and other relevant literature.
    • Before adding a substance or medication, verify that it is soluble and/or stable in Dextrose and Sodium Chloride Injection and that the pH range of Dextrose and Sodium Chloride Injection is appropriate.

    To Add Medication Before Solution Administration

    • 1. Prepare medication site.
    • 2. Using syringe with 19 to 22-gauge needle, puncture resealable medication port and inject.
    • 3. Mix solution and medication thoroughly. For high density medication such as potassium chloride, squeeze ports while ports are upright and mix thoroughly.
    • 4. After addition, check to ensure the solution is clear and there are no precipitates. Discard if there is a color change and/or the appearance of precipitates, insoluble complexes or crystals.

    To Add Medication During Solution Administration

    • 1. Close clamp on the set.
    • 2. Prepare medication site.
    • 3. Using syringe with 19 to 22-gauge needle, puncture resealable medication port and inject.
    • 4. Remove container from IV pole and/or turn to an upright position.
    • 5. Evacuate both ports by squeezing them while container is in the upright position.
    • 6. Mix solution and medication thoroughly.
    • 7. After addition, check to ensure the solution is clear and there are no precipitates. Discard if there is a color change and/or the appearance of precipitates, insoluble complexes or crystals, do not use.
    • 8. Return container to in use position and continue with administration.

    Storage

    • Use promptly; do not store solutions containing additives.
    • Single-dose container.
    • Discard any unused portion.
  • 3 DOSAGE FORMS AND STRENGTHS

    Dextrose and Sodium Chloride Injection are clear solutions in 250 mL, 500 mL and 1000 mL single-dose, flexible containers:

    250 mL flexible container

    • 5% Dextrose and 0.2% Sodium Chloride Injection, USP

    500 mL flexible container

    • 5% Dextrose and 0.2% Sodium Chloride Injection, USP
    • 5% Dextrose and 0.33% Sodium Chloride Injection, USP
    • 5% Dextrose and 0.45% Sodium Chloride Injection, USP
    • 5% Dextrose and 0.9% Sodium Chloride Injection, USP

    1000 mL flexible container

    • 2.5% Dextrose and 0.45% Sodium Chloride Injection, USP
    • 5% Dextrose and 0.2% Sodium Chloride Injection, USP
    • 5% Dextrose and 0.45% Sodium Chloride Injection, USP
    • 5% Dextrose and 0.9% Sodium Chloride Injection, USP
  • 4 CONTRAINDICATIONS

    Dextrose and Sodium Chloride Injection is contraindicated in patients with:

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Hypersensitivity Reactions

    Hypersensitivity and infusion reactions, including anaphylaxis, have been reported with Dextrose and Sodium Chloride Injection [see Adverse Reactions (6)]. Stop the infusion immediately if signs or symptoms of a hypersensitivity or infusion reaction develops [see Contraindications (4)]. Appropriate therapeutic countermeasures must be instituted as clinically indicated.

    5.2 Hyperglycemia and Hyperosmolar Hyperglycemic State

    The use of dextrose infusions in patients with impaired glucose tolerance may worsen hyperglycemia. Administration of dextrose at a rate exceeding the patient’s utilization rate may lead to hyperglycemia, coma, and death.

    Hyperglycemia is associated with an increase in serum osmolality, resulting in osmotic diuresis, dehydration and electrolyte losses. Patients with underlying central nervous system disease and renal impairment who receive dextrose infusions, may be at greater risk of developing hyperosmolar hyperglycemic state.

    Monitor blood glucose concentrations and treat hyperglycemia to maintain concentrations within normal limits while administering Dextrose and Sodium Chloride Injection. Insulin may be administered or adjusted to maintain optimal blood glucose concentrations.

    5.3 Hyponatremia

    Dextrose and Sodium Chloride Injection is a hypertonic solution [see Description, Table 1 (11)]. In the body, however, glucose containing fluids can become extremely physiologically hypotonic due to rapid glucose metabolization. Monitoring of serum sodium is particularly important for hypotonic fluids.

    Depending on the tonicity of the solution, the volume and rate of infusion, and depending on a patient’s underlying clinical condition and capability to metabolize glucose, intravenous administration of glucose can cause electrolyte disturbances, most importantly hypo- or hyperosmotic hyponatremia.

    The risk for hyponatremia is increased, in pediatric patients, elderly patients, postoperative patients, those with psychogenic polydipsia and in patients treated with medications that increase the risk of hyponatremia (such as certain diuretic, antiepileptic and psychotropic medications) [see Drug Interactions (7.1)].

    Acute hyponatremia can lead to acute hyponatremic encephalopathy characterized by headache, nausea, seizures, lethargy and vomiting. Patients with brain edema are at particular risk of severe, irreversible and life-threatening brain injury. Patients at increased risk for developing complications of hyponatremia, such as hyponatremic encephalopathy include pediatric patients; women, in particular, premenopausal women; patients with hypoxemia; and in patients with underlying central nervous system disease [see Use in Specific Populations (8.4, 8.5)].

    Avoid Dextrose and Sodium Chloride Injection in patients with or at risk for hyponatremia. If use cannot be avoided, monitor serum sodium concentrations.

    Rapid correction of hyponatremia is potentially dangerous with risk of serious neurologic complications such as osmotic demyelination syndrome with risk of seizures and cerebral edema. To avoid complications, monitor serum sodium and chloride concentrations, fluid status, acid-base balance, and signs of neurologic complications.

    High volume infusion must be used with close monitoring in patients with cardiac or pulmonary failure, and in patients with non-osmotic vasopressin release (including SIADH), due to the risk of hospital-acquired hyponatremia.

    5.4 Hypokalemia

    Excessive administration of Dextrose and Sodium Chloride Injection may result in significant hypokalemia. Hypokalemic periodic paralysis, metabolic alkalosis, increased gastrointestinal losses (e.g. diarrhea, vomiting), prolonged low potassium diet, or primary hyperaldosteronism may increase the risk of hypokalemia.Avoid the administration of Dextrose and Sodium Chloride Injection in patients with or at risk of hypokalemia or taking medications that may increase the risk. If use cannot be avoided, monitor serum potassium levels.

    5.5 Hypernatremia and Hyperchloremia

    Electrolyte imbalances such as hypernatremia and hyperchloremia, leading to metabolic acidosis may occur with solutions containing 0.9% sodium chloride.

    Conditions that may increase the risk of hypernatremia, fluid overload and edema (central and peripheral), include patients with pre-eclampsia, primary hyperaldosteronism and secondary hyperaldosteronism associated with, for example, hypertension, congestive heart failure, severe renal impairment, liver disease (including cirrhosis), and renal disease (including renal artery stenosis, nephrosclerosis).

    Medications such as corticosteroids or corticotropin, may increase the risk of sodium and fluid retention.

    Avoid in patients with or at risk for hypernatremia. If use cannot be avoided, monitor serum sodium concentrations.

    Rapid correction of hypernatremia is potentially dangerous with risk of serious neurologic complications. Excessively rapid correction of hypernatremia is also associated with a risk for serious neurologic complications such as osmotic demyelination syndrome (ODS) with risk of seizures and cerebral edema.

    5.6 Fluid Overload

    Depending on the volume and rate of infusion, the patient’s underlying clinical condition and capability to metabolize dextrose, intravenous administration of Dextrose and Sodium Chloride Injection can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations, overhydration, congested states or pulmonary edema.

    Avoid Dextrose and Sodium Chloride Injection in patients with or at risk for fluid and/or solute overloading. If use cannot be avoided, monitor fluid balance, electrolyte concentrations, and acid-base balance as needed and especially during prolonged use.

    5.7 Refeeding Syndrome

    Refeeding severely undernourished patients may result in the refeeding syndrome that is characterized by the shift of potassium, phosphorus, and magnesium intracellularly as the patient becomes anabolic. Thiamine deficiency and fluid retention may also develop. To prevent these complications, monitor severely undernourished patients and slowly increasing nutrient intake.

  • 6 ADVERSE REACTIONS

    - Anaphylactic reaction, hypersensitivity, and chills

    - Hyponatremia (applies to solutions containing less than 0.9% Sodium Chloride)

    Reactions which may occur because of the solution or the technique of administration include febrile response, infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection, extravasation and hypervolemia.

    If an adverse reaction does occur, discontinue the infusion, evaluate the patient, institute appropriate therapeutic countermeasures and save the remainder of the fluid for examination if deemed necessary.

  • 7 DRUG INTERACTIONS

    7.1 Other Products that Affect Glycemic Control, Vasopressin or Fluid and/or Electrolyte Balance

    Dextrose and Sodium Chloride Injection can affect glycemic control, vasopressin and fluid and/or electrolyte balance [see Warnings and Precautions (5.2, 5.3, 5.4, 5.5, 5.6)]. Monitor blood glucose concentrations, fluid balance, serum electrolyte concentrations and acid-base balance when using Dextrose and Sodium Chloride Injection in patients treated with other substances that affect glycemic control, vasopressin or fluid and/or electrolyte balance.

    7.2 Lithium

    Renal sodium and lithium clearance may be increased during administration of Dextrose and Sodium Chloride Injection resulting in decreased serum lithium concentrations. Monitor serum lithium concentrations during concomitant use.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    Appropriate administration of Dextrose and Sodium Chloride Injection during pregnancy is not expected to cause adverse developmental outcomes, including congenital malformations. Animal reproduction studies have not been conducted with Dextrose and Sodium Chloride Injection.

    The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively.

    8.2 Lactation

    Risk Summary

    Sodium is present in human breast milk. There are no data on the effects of Dextrose and Sodium Chloride Injection on a breastfed infant or the effects on milk production.

    The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for Dextrose and Sodium Chloride Injection and any potential adverse effects on the breastfed infant from Dextrose and Sodium Chloride Injection or from the underlying maternal condition.

    8.4 Pediatric Use

    The safety profile of Dextrose and Sodium Chloride Injection in pediatric patients is similar to adults.

    Neonates, especially premature infants with low birth weight, are at increased risk of developing hypo- or hyperglycemia and therefore need close monitoring during treatment with intravenous glucose solutions to ensure adequate glycemic control in order to avoid potential long-term adverse effects.

    Closely monitor plasma electrolyte concentrations in pediatric patients who may have impaired ability to regulate fluids and electrolytes. In very low birth weight infants, excessive or rapid administration of Dextrose and Sodium Chloride Injection may result in increased serum osmolality and risk of intracerebral hemorrhage.

    Children (including neonates and older children) are at increased risk of developing hyponatremia as well as for developing hyponatremic encephalopathy.

    8.5 Geriatric Use

    Clinical studies of Dextrose and Sodium Chloride Injection did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects.

    Elderly patients are at increased risk of developing hyponatremia as well as for developing hyponatremic encephalopathy [see Warnings and Precautions (5.3)]. Dextrose and Sodium Chloride Injection is known to be substantially excreted by the kidney, and the risk of adverse reactions to this product may be greater in patients with impaired renal function [see Warnings and Precautions (5.2, 5.5)].

    Dose selection for an elderly patient should be cautious, starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.

    8.6 Renal Impairment

    Administration of Dextrose and Sodium Chloride Injection in patients with renal impairment may result in hyperosmolar hyperglycemic state, hyponatremia, and/or fluid overload. Monitor patients with renal impairment for development of these adverse reactions [see Warnings and Precautions (5.2, 5.3, 5.5, 5.6)].

  • 10 OVERDOSAGE

    Excessive administration of Dextrose and Sodium Chloride Injection can cause:

    Electrolyte and Fluid Disorders

    When assessing an overdose, any additives in the solution must also be considered. Clinically significant overdose of Dextrose and Sodium Chloride Injection may, therefore, constitute a medical emergency. The effects of an overdose may require immediate medical attention and treatment.

    Interventions include discontinuation of the infusion, dose reduction, monitoring of fluid balance, electrolyte concentrations and acid-base balance and institution of appropriate corrective measures such as administration of exogenous insulin.

  • 11 DESCRIPTION

    Dextrose and Sodium Chloride Injection, USP is a sterile, nonpyrogenic solution for fluid and electrolyte replenishment and caloric supply in single-dose containers for intravenous administration. It contains no antimicrobial agents. Composition, osmolarity, pH, ionic concentration and caloric content are shown in Table 1.

    Table 1.
  • * Normal physiologic osmolarity range is approximately 280 to 310 mOsmol/L.
  • Size (mL)

    Composition (g/L)

    *Osmolarity (mOsmol/L) (calc.)

    pH

    Ionic Concentration (mEq/L)

    Caloric Content
    (kcal/L)

    **Dextrose Hydrous,
    USP

    Sodium Chloride, USP
    (NaCl)

    Sodium

    Chloride

    2.5% Dextrose and 0.45% Sodium Chloride Injection, USP

    1000

    25

    4.5

    280

    4.5

    (3.2 to 6.5)

    77

    77

    85

    5% Dextrose and 0.2% Sodium Chloride Injection, USP

    250

    500

    1000

    50

    2

    321

    4.0

    (3.2 to 6.5)

    34

    34

    170

    5% Dextrose and 0.33% Sodium Chloride Injection, USP

    250

    500

    1000

    50

    3.3

    365

    4.0

    (3.2 to 6.5)

    56

    56

    170

    5% Dextrose and 0.45% Sodium Chloride Injection, USP

    500

    1000

    50

    4.5

    406

    4.0

    (3.2 to 6.5)

    77

    77

    170

    5% Dextrose and 0.9% Sodium Chloride Injection, USP

    500

    1000

    50

    9

    560

    4.0

    (3.2 to 6.5)

    154

    154

    170

    Dextrose Structural Formula

    Dextrose is derived from corn.

    The VIAFLEX Plus plastic container is fabricated from a specially formulated polyvinyl chloride (PL 146 Plastic). The amount of water that can permeate from inside the container into the overwrap is insufficient to affect the solution significantly. Solutions in contact with the plastic container can leach out certain of its chemical components in very small amounts within the expiration period, e.g., di-2-ethylhexyl phthalate (DEHP), up to 5 parts per million. However, the safety of the plastic has been confirmed in tests in animals according to USP biological tests for plastic containers as well as by tissue culture toxicity studies.

  • 12 CLINICAL PHARMACOLOGY

    Dextrose and Sodium Chloride Injection, USP has value as a source of water, electrolytes, and calories. It is capable of inducing diuresis depending on the clinical condition of the patient.

    12.1 Mechanism of Action

    Dextrose and Sodium Chloride Injection is a source of water, electrolytes and calories. It is capable of inducing diuresis depending on the clinical condition of the patient.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    Dextrose and Sodium Chloride Injection are clear solutions in 250 mL, 500 mL and 1000 mL single-dose, flexible containers available as follows:

    Code

    Size (mL)

    NDC

    Product Name

    2B1024

    1000

    0338-0073-04

    2.5% Dextrose and 0.45% Sodium Chloride Injection, USP

    2B1092

    250

    0338-0077-02

    5% Dextrose and 0.2% Sodium Chloride Injection, USP

    2B1093

    500

    0338-0077-03

    2B1094

    1000

    0338-0077-04

    2B1083

    500

    0338-0081-03

    5% Dextrose and 0.33% Sodium Chloride Injection, USP

    2B1073

    500

    0338-0085-03

    5% Dextrose and 0.45% Sodium Chloride Injection, USP

    2B1074

    1000

    0338-0085-04

    2B1063

    500

    0338-0089-03

    5% Dextrose and 0.9% Sodium Chloride Injection, USP

    2B1064

    1000

    0338-0089-04

    Storage: Avoid excessive heat. Store at room temperature (25°C/77°F); brief exposure up to 40°C/104°F does not adversely affect the product.

  • 17 PATIENT COUNSELING INFORMATION

    Inform patients, caregivers or home healthcare providers of the following risks of Dextrose and Sodium Chloride Injection:

    Baxter Healthcare Corporation
    Deerfield, IL 60015 USA
    Printed in USA

    Distributed in Canada by
    Baxter Corporation
    Mississauga, ON L5N 0C2

    07-19-74-506

    Baxter, and Viaflex and PL 146 are trademarks of Baxter International Inc.

    For Product Information
    1-800-933-0303

  • PACKAGE/LABEL PRINCIPAL DISPLAY PANEL

    Dextrose and Sodium Chloride Representative Container Label NDC: <a href=/NDC/0338-0089-03>0338-0089-03</a>

    Container Label

    Container Label

    LOT EXP

    2B1063
    NDC: 0338-0089-03

    5% Dextrose and
    0.9% Sodium Chloride
    Injection USP

    500 mL EACH 100 mL CONTAINS 5 g DEXTROSE HYDROUS USP
    900 mg SODIUM CHLORIDE USP pH 4.0 (3.2 TO 6.5)
    mEq/L SODIUM 154 CHLORIDE 154 HYPERTONIC
    OSMOLARITY 560 mOsmol/L (CALC) STERILE
    NONPYROGENIC SINGLE DOSE CONTAINER ADDITIVES MAY BE
    INCOMPATIBLE CONSULT WITH PHARMACIST IF AVAILABLE
    WHEN INTRODUCING ADDITIVES USE ASEPTIC TECHNIQUE MIX
    THOROUGHLY DO NOT STORE DOSAGE INTRAVENOUSLY AS
    DIRECTED BY A PHYSICIAN SEE DIRECTIONS CAUTIONS
    SQUEEZE AND INSPECT INNER BAG WHICH MAINTAINS PRODUCT
    STERILITY DISCARD IF LEAKS ARE FOUND MUST NOT BE USED
    IN SERIES CONNECTIONS DO NOT USE UNLESS SOLUTION IS
    CLEAR RX ONLY STORE UNIT IN MOISTURE BARRIER
    OVERWRAP AT ROOM TEMPERATURE (25°C/77°F) UNTIL READY
    TO USE AVOID EXCESSIVE HEAT SEE INSERT

    VIAFLEX CONTAINER PL 146 PLASTIC

    BAXTER VIAFLEX AND PL 146 ARE TRADEMARKS OF
    BAXTER INTERNATIONAL INC

    FOR PRODUCT INFORMATION 1-800-933-0303

    BAXTER Logo
    BAXTER HEALTHCARE CORPORATION
    DEERFIELD IL 60015 USA

    MADE IN USA

    1

    2

    3

    4

    Dextrose & Sodium Chloride Representatve Carton Label NDC: <a href=/NDC/0338-0089-03>0338-0089-03</a>6

    Carton Label

    Carton Label

    2B1063Q 24-500 ML

    VIAFLEX® CONTAINER

    5% DEXTROSE AND
    0.9% SODIUM CHLORIDE INJ, USP

    EXP
    XXXXX

    SECONDARY BAR CODE
    (17) YYMM00 (10) XXXXX

    LOT
    XXXXX

    PRIMARY BAR CODE
    (01) 50303380089036

    Dextrose & Sodium Chloride Representative Container Label NDC  0338-0073-04

    Container Label

    Container Label

    LOT EXP

    2B1024
    NDC: 0338-0073-04

    2.5% Dextrose
    and 0.45%
    Sodium Chloride
    Injection USP

    1000 mL

    EACH 100 mL CONTAINS 2.5 g DEXTROSE HYDROUS USP
    450 mg SODIUM CHLORIDE USP pH 4.0 (3.2 TO 6.5)
    mEq/L SODIUM 77 CHLORIDE 77 OSMOLARITY 280
    mOsmol/L (CALC) STERILE NONPYROGENIC SINGLE
    DOSE CONTAINER ADDITIVES MAY BE INCOMPATIBLE
    CONSULT WITH PHARMACIST IF AVAILABLE WHEN
    INTRODUCING ADDITIVES USE ASEPTIC TECHNIQUE MIX
    THOROUGHLY DO NOT STORE DOSAGE INTRAVENOUSLY
    AS DIRECTED BY A PHYSICIAN SEE DIRECTIONS CAUTIONS
    SQUEEZE AND INSPECT INNER BAG WHICH MAINTAINS
    PRODUCT STERILITY DISCARD IF LEAKS ARE FOUND MUST
    NOT BE USED IN SERIES CONNECTIONS DO NOT USE UNLESS
    SOLUTION IS CLEAR RX ONLY STORE UNIT IN MOISTURE
    BARRIER OVERWRAP AT ROOM TEMPERATURE (25°C/77°F)
    UNTIL READY TO USE AVOID EXCESSIVE HEAT SEE INSERT

    VIAFLEX CONTAINER PL 146 PLASTIC

    BAXTER VIAFLEX AND PL 146 ARE TRADEMARKS OF
    BAXTER INTERNATIONAL INC

    FOR PRODUCT INFORMATION 1-800-933-0303

    Baxter Logo
    BAXTER HEALTHCARE CORPORATION
    DEERFIELD IL 60015 USA
    MADE IN USA

    1

    2

    3

    4

    5

    6

    7

    8

    9

    Dextrose & Sodium Chloride Representative Carton Label NDC: <a href=/NDC/0338-0073-04>0338-0073-04</a>2

    Carton Label

    Carton Label

    2B1024X 14-1000 ML

    VIAFLEX® CONTAINER

    2.5% DEXTROSE AND
    0.45% SODIUM CHLORIDE INJ, USP

    EXP
    XXXXX

    SECONDARY BAR CODE
    (17) XXXXX (10) XXXXX

    LOT
    XXXXX

    PRIMARY BAR CODE
    (01) 50303380073042

    Dextrose & Sodium Chloride Representative Container Label NDC: <a href=/NDC/0338-0077-02>0338-0077-02</a>

    Container Label

    Container Label

    LOT EXP

    2B1092
    NDC: 0338-0077-02

    5% Dextrose and
    0.2% Sodium Chloride
    Injection USP

    250 mL EACH 100 mL CONTAINS
    5 g DEXTROSE HYDROUS
    USP 200 mg SODIUM CHLORIDE USP
    pH 4.0 (3.2 TO 6.5) mEq/L SODIUM 34
    CHLORIDE 34 OSMOLARITY 321 mOsmol/L
    (CALC) STERILE NONPYROGENIC SINGLE
    DOSE CONTAINER ADDITIVES MAY BE
    INCOMPATIBLE CONSULT WITH PHARMACIST
    IF AVAILABLE WHEN INTRODUCING ADDITIVES
    USE ASEPTIC TECHNIQUE MIX THOROUGHLY
    DO NOT STORE DOSAGE INTRAVENOUSLY AS
    DIRECTED BY A PHYSICIAN SEE DIRECTIONS
    CAUTIONS SQUEEZE AND INSPECT INNER
    BAG WHICH MAINTAINS PRODUCT STERILITY
    DISCARD IF LEAKS ARE FOUND MUST NOT BE
    USED IN SERIES CONNECTIONS DO NOT
    USE UNLESS SOLUTION IS CLEAR RX
    ONLY STORE UNIT IN MOISTURE BARRIER
    OVERWRAP AT ROOM TEMPERATURE
    (25°C/77°F) UNTIL READY TO USE AVOID
    EXCESSIVE HEAT SEE INSERT

    VIAFLEX CONTAINER PL 146 PLASTIC

    BAXTER VIAFLEX AND PL 146 ARE
    TRADEMARKS OF BAXTER INTERNATIONAL INC

    FOR PRODUCT INFORMATION
    1-800-933-0303

    BAXTER Logo
    BAXTER HEALTHCARE CORPORATION
    DEERFIELD IL 60015 USA
    MADE IN USA

    50

    100

    150

    200

    Dextrose and Sodium Chloride Representative Carton Label 0338-0077-02

    Carton Label

    Carton Label

    Carton Label

    2B1092Q 36-250 ML

    VIAFLEX® CONTAINER

    5% DEXTROSE AND
    0.2% SODIUM CHLORIDE INJ, USP

    EXP
    XXXXX

    SECONDARY BAR CODE
    (17) YYMM00 (10) XXXXX

    LOT
    XXXXX

    PRIMARY BAR CODE
    (01) 50303380077026

    Dextrose and Sodium Chloride Representative Container Label 0338-0081-03

    Container Label

    Container Label

    Container Label

    LOT EXP

    2B1083
    NDC: 0338-0081-03

    5% Dextrose and
    0.33% Sodium Chloride
    Injection USP

    500 mL

    EACH 100 mL CONTAINS 5 g DEXTROSE HYDROUS USP
    330 mg SODIUM CHLORIDE USP pH 4.0 (3.2 TO 6.5)
    mEq/L SODIUM 56 CHLORIDE 56 OSMOLARITY 356
    mOsmol/L (CALC) STERILE NONPYROGENIC SINGLE DOSE
    CONTAINER ADDITIVES MAY BE INCOMPATIBLE CONSULT WITH
    PHARMACIST IF AVAILABLE WHEN INTRODUCING ADDITIVES USE
    ASEPTIC TECHNIQUE MIX THOROUGHLY DO NOT STORE
    DOSAGE INTRAVENOUSLY AS DIRECTED BY A PHYSICIAN SEE
    DIRECTIONS CAUTIONS SQUEEZE AND INSPECT INNER BAG
    WHICH MAINTAINS PRODUCT STERILITY DISCARD IF LEAKS ARE
    FOUND MUST NOT BE USED IN SERIES CONNECTIONS DO NOT
    USE UNLESS SOLUTION IS CLEAR RX ONLY STORE UNIT IN
    MOISTURE BARRIER OVERWRAP T ROOM TEMPERATURE
    (25°C/77°F) UNTIL READY TO USE AVOID EXCESSIVE HEAT
    SEE INSERT

    VIAFLEX CONTAINER PL 146 PLASTIC

    BAXTER VIAFLEX AND PL 146 ARE TRADEMARKS OF
    BAXTER INTERNATIONAL INC

    FOR PRODUCT INFORMATION 1-800-933-0303

    Baxter Logo
    BAXTER HEALTHCARE CORPORATION
    DEERFIELD IL 60015 USA

    MADE IN USA

    07-25-34-096

    1

    2

    3

    4

    Dextrose and Sodium Chloride Representative Carton Label 0338-0081-03

    Carton Label

    Carton Label

    2B1083Q 24-500 ML

    VIAFLEX® CONTAINER

    5% DEXTROSE AND
    0.33% SODIUM CHLORIDE INJ, USP

    EXP
    XXXXX

    SECONDARY BAR CODE
    (17) XXXXX (10) XXXXX

    LOT
    XXXXX

    PRIMARY BAR CODE
    (01) 50303380081030

    Dextrose & Sodium Chloride Representative Container Label NDC: <a href=/NDC/0338-0085-03>0338-0085-03</a>

    Container Label

    Container Label

    LOT EXP

    2B1073
    NDC: 0338-0085-03

    5% Dextrose and
    0.45% Sodium Chloride
    Injection USP

    500 mL

    EACH 100 mL CONTAINS 5 g DEXTROSE HYDROUS USP
    450 mg SODIUM CHLORIDE USP pH 4.0 (3.2 TO 6.5)
    mEq/L SODIUM 77 CHLORIDE 77 HYPERTONIC OSMOLARITY
    406 mOsmol/L (CALC) STERILE NONPYROGENIC SINGLE
    DOSE CONTAINER ADDITIVES MAY BE INCOMPATIBLE CONSULT
    WITH PHARMACIST IF AVAILABLE WHEN INTRODUCING ADDITIVES
    USE ASEPTIC TECHNIQUE MIX THOROUGHLY DO NOT STORE
    DOSAGE INTRAVENOUSLY AS DIRECTED BY A PHYSICIAN SEE
    DIRECTIONS CAUTIONS SQUEEZE AND INSPECT INNER BAG
    WHICH MAINTAINS PRODUCT STERILITY DISCARD IF LEAKS ARE
    FOUND MUST NOT BE USED IN SERIES CONNECTIONS DO NOT
    USE UNLESS SOLUTION IS CLEAR RX ONLY STORE UNIT IN
    MOISTURE BARRIER OVERWRAP AT ROOM TEMPERATURE
    (25°C/77°F) UNTIL READY TO USE AVOID EXCESSIVE HEAT
    SEE INSERT

    VIAFLEX CONTAINER PL 146 PLASTIC

    BAXTER VIAFLEX AND PL 146 ARE
    TRADEMARKS OF BAXTER INTERNATIONAL INC

    FOR PRODUCT INFORMATION 1-800-933-0303

    BAXTER Logo
    BAXTER HEALTHCARE CORPORATION
    DEERFIELD IL 60015 USA

    MADE IN USA

    1

    2

    3

    4

    Dextrose & Sodium Chloride Representative Carton Label NDC: <a href=/NDC/0338-0085-03>0338-0085-03</a>8

    Carton Label

    Carton Label

    2B1073Q 24-500 ML

    VIAFLEX® CONTAINER

    5% DEXTROSE AND
    0.45% SODIUM CHLORIDE INJ, USP

    EXP
    XXXXX

    SECONDARY BAR CODE
    (17) YYMM00 (10) XXXXX

    LOT
    XXXXX

    PRIMARY BAR CODE
    (01) 50303380085038

  • INGREDIENTS AND APPEARANCE
    DEXTROSE AND SODIUM CHLORIDE 
    dextrose and sodium chloride injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0338-0073
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE2.5 g  in 100 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE450 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0338-0073-0414 in 1 CARTON03/22/1971
    11000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA01669703/22/1971
    DEXTROSE AND SODIUM CHLORIDE 
    dextrose and sodium chloride injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0338-0077
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE5 g  in 100 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE200 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0338-0077-0236 in 1 CARTON12/08/1970
    1250 mL in 1 BAG; Type 0: Not a Combination Product
    2NDC: 0338-0077-0324 in 1 CARTON12/08/1970
    2500 mL in 1 BAG; Type 0: Not a Combination Product
    3NDC: 0338-0077-0414 in 1 CARTON12/08/1970
    31000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA01668912/08/1970
    DEXTROSE AND SODIUM CHLORIDE 
    dextrose and sodium chloride injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0338-0081
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE5 g  in 100 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE330 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0338-0081-0324 in 1 CARTON03/22/1971
    1500 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA01668703/22/1971
    DEXTROSE AND SODIUM CHLORIDE 
    dextrose and sodium chloride injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0338-0085
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE5 g  in 100 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE450 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0338-0085-0324 in 1 CARTON03/22/1971
    1500 mL in 1 BAG; Type 0: Not a Combination Product
    2NDC: 0338-0085-0414 in 1 CARTON03/22/1971
    21000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA01668303/22/1971
    DEXTROSE AND SODIUM CHLORIDE 
    dextrose and sodium chloride injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0338-0089
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE5 g  in 100 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE900 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0338-0089-0324 in 1 CARTON12/09/1970
    1500 mL in 1 BAG; Type 0: Not a Combination Product
    2NDC: 0338-0089-0414 in 1 CARTON12/09/1970
    21000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA01667812/09/1970
    Labeler - Baxter Healthcare Corporation (005083209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Baxter Healthcare Corporation059140764MANUFACTURE(0338-0073, 0338-0077, 0338-0081, 0338-0085, 0338-0089) , ANALYSIS(0338-0073, 0338-0077, 0338-0081, 0338-0085, 0338-0089) , LABEL(0338-0073, 0338-0077, 0338-0081, 0338-0085, 0338-0089) , PACK(0338-0073, 0338-0077, 0338-0081, 0338-0085, 0338-0089) , STERILIZE(0338-0073, 0338-0077, 0338-0081, 0338-0085, 0338-0089)
    Establishment
    NameAddressID/FEIBusiness Operations
    Baxter Healthcare Corporation194684502ANALYSIS(0338-0073, 0338-0077, 0338-0081, 0338-0085, 0338-0089)

  • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.