Label: MAGNESIUM SULFATE IN WATER injection, solution

  • NDC Code(s): 0409-6729-03, 0409-6729-09, 0409-6729-11, 0409-6729-21, view more
    0409-6729-23, 0409-6729-24, 0409-6729-31, 0409-6729-41, 0409-6730-11, 0409-6730-13
  • Packager: Hospira, Inc.
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated June 24, 2020

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Flexible Plastic Container

    For Intravenous Use Only

    Rx only

  • DESCRIPTION

    Magnesium Sulfate in Water for Injection is a sterile, nonpyrogenic solution of magnesium sulfate heptahydrate in water for injection. May contain sulfuric acid and/or sodium hydroxide for pH adjustment. The pH is 4.5 (3.5 to 6.5). It is available in 4% and 8% concentrations. See HOW SUPPLIED section for the content and characteristics of available dosage forms and sizes.

    Magnesium Sulfate, USP heptahydrate is chemically designated MgSO4 • 7H2O, colorless crystals or white powder freely soluble in water.

    Water for Injection, USP is chemically designated H2O.

    The flexible plastic container is fabricated from a specially formulated polyvinylchloride. Water can permeate from inside the container into the overwrap but not in amounts sufficient to affect the solution significantly. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials. Exposure to temperatures above 25°C/77°F during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.

  • CLINICAL PHARMACOLOGY

    Magnesium (Mg++) is an important cofactor for enzymatic reactions and plays an important role in neurochemical transmission and muscular excitability.

    Magnesium prevents or controls convulsions by blocking neuromuscular transmission and decreasing the amount of acetylcholine liberated at the end plate by the motor nerve impulse. Magnesium is said to have a depressant effect on the central nervous system, but it does not adversely affect the mother, fetus or neonate when used as directed in eclampsia or pre-eclampsia. Normal serum magnesium levels range from 1.3 to 2.1 mEq/liter.

    As serum magnesium rises above 4 mEq/liter, the deep tendon reflexes are first decreased and then disappear as the serum level approaches 10 mEq/liter. At this level respiratory paralysis may occur. Heart block also may occur at this or lower serum levels of magnesium.

    Magnesium acts peripherally to produce vasodilation. With low doses only flushing and sweating occur, but larger doses cause lowering of blood pressure. The central and peripheral effects of magnesium poisoning are antagonized to some extent by intravenous administration of calcium.

    With intravenous administration the onset of anticonvulsant action is immediate and lasts about 30 minutes. Following intramuscular administration the onset of action occurs in about one hour and persists for three to four hours. Effective anticonvulsant serum levels range from 2.5 to 7.5 mEq/liter.

    Pharmacokinetics:

    Absorption: Intravenously administered magnesium is immediately absorbed.

    Distribution: Approximately 1-2% of total body magnesium is located in the extracellular fluid space. Magnesium is 30% bound to albumin.

    Metabolism: Magnesium is not metabolized.

    Excretion: Magnesium is excreted solely by the kidney at a rate proportional to the serum concentration and glomerular filtration.

    Special Populations:

    Renal Insufficiency: Magnesium is excreted solely by the kidney. In patients with severe renal insufficiency, the dose should be lower and frequent serum magnesium levels must be obtained (see DOSAGE AND ADMINISTRATION).

    Hepatic Insufficiency: Magnesium is excreted solely by the kidney. No dosing adjustments are necessary in hepatic insufficiency.

    Drug-Drug Interactions: Drug induced renal losses of magnesium occur with the following drugs or drug classes:

         Aminoglycosides                                   Amphotericin B
         Cyclosporine                                         Diuretics
         Digitalis                                                 Cisplatin
         Alcohol

  • INDICATIONS AND USAGE

    Magnesium Sulfate in Water for Injection is indicated for the prevention and control of seizures in preeclampsia and eclampsia, respectively. When used judiciously it effectively prevents and controls the convulsions of eclampsia without producing deleterious depression of the central nervous system of the mother or infant. However, other effective drugs are available for this purpose.

  • CONTRAINDICATIONS

    Intravenous magnesium should not be given to mothers with toxemia of pregnancy during the two hours preceding delivery.

  • WARNINGS

    FETAL HARM: Continuous administration of magnesium sulfate beyond 5-7 days to pregnant women can lead to hypocalcemia and bone abnormalities in the developing fetus. These bone abnormalities include skeletal demineralization and osteopenia. In addition, cases of neonatal fracture have been reported. The shortest duration of treatment that can lead to fetal harm is not known.   Magnesium sulfate should be used during pregnancy only if clearly needed.  If magnesium sulfate is given for treatment of preterm labor, the woman should be informed that the efficacy and safety of such use have not been established and that use of magnesium sulfate beyond 5-7 days may cause fetal abnormalities.

    Parenteral use in the presence of renal insufficiency may lead to magnesium intoxication.

  • PRECAUTIONS

    Because magnesium is removed from the body solely by the kidneys, the drug should be used with caution in patients with renal impairment. Urine output should be maintained at a level of 100 mL every four hours. Monitoring serum magnesium levels and the patient’s clinical status is essential to avoid the consequences of overdosage in toxemia. Clinical indications of a safe dosage regimen include the presence of the patellar reflex (knee jerk) and absence of respiratory depression (approximately 16 breaths or more/minute). Serum magnesium levels usually sufficient to control convulsions range from 3 to 6 mg/100 mL (2.5 to 5 mEq/liter). The strength of the deep tendon reflexes begins to diminish when serum magnesium levels exceed 4 mEq/liter. Reflexes may be absent at 10 mEq magnesium/liter, where respiratory paralysis is a potential hazard. An injectable calcium salt should be immediately available to counteract the potential hazards of magnesium intoxication in eclampsia.

    Magnesium Sulfate in Water for Injection should be administered slowly to avoid producing hypermagnesemia.

    Carcinogenesis, Mutagenesis, Impairment of Fertility: Studies with Magnesium Sulfate in Water for Injection have not been performed to evaluate carcinogenic potential, mutagenic potential or effects on fertility.

    Pregnancy (See WARNINGS and PRECAUTIONS)

    Teratogenic Effects:

    Magnesium Sulfate in Water for Injection, can cause fetal abnormalities when administered beyond 5-7 days to pregnant women. There are retrospective epidemiological studies and case reports documenting fetal abnormalities such as hypocalcemia, skeletal demineralization’s, osteopenia and other l skeletal abnormalities with continuous maternal administration of magnesium sulfate for more than 5-7 days.1-12 Magnesium Sulfate in Water for Injection should be used during pregnancy only if clearly needed. If this drug is used during pregnancy the woman should be apprised of the potential harm to the fetus.

    Nonteratogenic Effects:

    When administered by continuous IV infusion (especially for more than 24 hours preceding delivery) to control convulsions in a toxemic woman, the newborn may show signs of magnesium toxicity, including neuromuscular or respiratory depression. (See OVERDOSAGE.)

    Labor and Delivery:

    Continuous administration of magnesium sulfate is an unapproved treatment for preterm labor. The safety and efficacy of such use have not been established. The administration of Magnesium Sulfate in Water for Injection outside of its approved indication in pregnant women should be by trained obstetrical personnel in a hospital setting with appropriate obstetrical care facilities.

    Nursing Mothers:

    It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Magnesium Sulfate in Water for Injection is administered to a nursing mother.

  • ADVERSE REACTIONS

    The adverse effects of parenterally administered magnesium usually are the result of magnesium intoxication. These include flushing, sweating, hypotension, depressed reflexes, flaccid paralysis, hypothermia, circulatory collapse, cardiac and central nervous system depression proceeding to respiratory paralysis.

    Hypocalcemia with signs of tetany secondary to magnesium sulfate therapy for eclampsia has been reported.

  • OVERDOSAGE

    Magnesium intoxication is manifested by a sharp drop in blood pressure and respiratory paralysis. Disappearance of the patellar reflex is a useful clinical sign to detect the onset of magnesium intoxication. In the event of overdosage, artificial ventilation must be provided until a calcium salt can be injected IV to antagonize the effects of magnesium.

    For Treatment of Overdose

    Artificial respiration is often required. Intravenous calcium, 10 to 20 mL of a 5% solution (diluted if desirable) with isotonic sodium chloride for injection) is used to counteract effects of hypermagnesemia. Subcutaneous physostigmine, 0.5 to 1 mg may be helpful.

    Hypermagnesemia in the newborn may require resuscitation and assisted ventilation via endotracheal intubation or intermittent positive pressure ventilation as well as IV calcium.

  • DOSAGE AND ADMINISTRATION

    Magnesium Sulfate in Water for Injection is intended for intravenous use only. For the management of pre-eclampsia or eclampsia, intravenous infusions of dilute solutions of magnesium (1% to 8%) are often given in combination with intramuscular injections of 50% Magnesium Sulfate Injection, USP. Therefore, in the clinical conditions cited below, both forms of therapy are noted, as appropriate.

    Continuous maternal administration of magnesium sulfate in pregnancy beyond 5-7 days can cause fetal abnormalities.

    In Eclampsia

    In severe pre-eclampsia or eclampsia, the total initial dose is 10 to 14 g of magnesium sulfate. To initiate therapy, 4 g of Magnesium Sulfate in Water for Injection may be administered intravenously. The rate of I.V. infusion should generally not exceed 150 mg/minute, or 3.75 mL of a 4% concentration (or its equivalent) per minute, except in severe eclampsia with seizures. Simultaneously, 4 to 5 g (32.5 to 40.6 mEq) of magnesium sulfate may be administered intramuscularly into each buttock using undiluted 50% Magnesium Sulfate Injection, USP. After the initial I.V. dose, some clinicians administer 1 to 2 g/hour by constant I.V. infusion.

    Subsequent intramuscular doses of 4 to 5 g of magnesium sulfate may be injected into alternate buttocks every four hours, depending on the continuing presence of the patellar reflex, adequate respiratory function, and absence of signs of magnesium toxicity. Therapy should continue until paroxysms cease.

    A serum magnesium level of 6 mg/100 mL is considered optimal for control of seizures. A total daily (24 hr) dose of 30 to 40 g magnesium sulfate should not be exceeded. In the presence of severe renal insufficiency, frequent serum magnesium concentrations must be obtained and the maximum dosage of magnesium sulfate is 20 g per 48 hours.

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

    Do not administer unless solution is clear. Discard unused portion.

  • HOW SUPPLIED

    Magnesium Sulfate in Water for Injection is supplied in single-dose flexible plastic containers as follows:

    NDC No.

    Size
    Container

    Total
    Magnesium
    Sulfate**

    Total
    Magnesium
    Ion

    Magnesium
    Sulfate**
    Concentration

    Magnesium Ion
    Concentration

    Osmolarity (calc.)

    0409-6729-23

       100 mL

       4 g

       32.5 mEq

    4% (40 mg/mL)

    32.5 mEq/100 mL

    325 mOsmol/Liter

    0409-6729-03

       500 mL

    20 g

    162.3 mEq

    4% (40 mg/mL)

    32.5 mEq/100 mL

    325 mOsmol/Liter

    0409-6729-09

    1000 mL

    40 g

       325 mEq

    4% (40 mg/mL)

    32.5 mEq/100 mL

    325 mOsmol/Liter

    0409-6729-24

           50 mL*

       2 g

    16.25 mEq

    4% (40 mg/mL)

    16.25 mEq/50 mL

    325 mOsmol/Liter

    0409-6730-13

           50 mL*

       4 g

        32.5 mEq

    8% (80 mg/mL)

      32.5 mEq/50 mL

    649 mOsmol/Liter

      * Partial fill container 50 mL volume in 100 mL container.
    ** As the heptahydrate.

    WARNING: DO NOT USE FLEXIBLE CONTAINER IN SERIES CONNECTIONS.

    Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.] Protect from freezing.

  • REFERENCES

    1. Yokoyama K, Takahashi N, Yada Y. Prolonged maternal magnesium administration and bone metabolism in neonates. Early Human Dev. 2010; 86(3):187-91. Epub 2010 Mar 12.
    2. Wedig KE, Kogan J, Schorry EK et al. Skeletal demineralization and fractures caused by fetal magnesium toxicity. J Perinatol. 2006; 26(6):371-4.
    3. Nassar AH, Sakhel K, Maarouf H, et al. Adverse maternal and neonatal outcome of prolonged course of magnesium sulfate tocolysis. Acta Obstet Gynecol Scan. 2006;85(9):1099-103.
    4. Malaeb SN, Rassi A, Haddad MC. Bone mineralization in newborns whose mothers received magnesium sulphate for tocolysis of premature labor. Pediatr Radiol. 2004;34(5):384-6. Epub 2004 Feb 18.
    5. Matsuda Y, Maeda Y, Ito M, et al. Effect of magnesium sulfate treatment on neonatal bone abnormalities. Gynecol Obstet Invest. 1997; 44(2):82-8.
    6. Schanler RJ, Smith LG, Burns PA. Effects of long-term maternal intravenous magnesium sulfate therapy on neonatal calcium metabolism and bone mineral content. Gynecol Obstet Invest. 1997; 43(4):236-41.
    7. Santi MD, Henry GW, Douglas GL. Magnesium sulfate treatment of preterm labor as a cause of abnormal neonatal bone mineralization. J Pediatr Orthop. 1994; 14(2):249-53.
    8. Holocomb WL, Shackelford GD, Petrie RH. Magnesium tocolysis and neonatal bone abnormalities: a controlled study. Obstet Gynecol. 1991; 78(4):611-4.
    9. Cumming WA, Thomas VJ. Hypermagnesemia: a cause of abnormal metaphyses in the neonate. Am J Roentgenol. 1989; 152(5):1071-2.
    10. Lamm CL, Norton KL, Murphy RJ. Congenital rickets associated with magnesium sulfate infusion for tocolysis. J Pediatr. 1988; 113(6):1078-82.
    11. McGuinness GA, Weinstein MM, Cruikshank DP, et al. Effects of magnesium sulfate treatment on perinatal calcium metabolism. II. Neonatal responses. Obstet Gynecol. 1980;56(5):595-600.
    12. Riaz M, Porat R, Brodsky NL, et al. The effect of maternal magnesium sulfate treatment on newborns: a prospective controlled study. J Perinatol. 1998; 18(6 pt 1):449-54.

    Logo

    Distributed by Hospira, Inc., Lake Forest, IL 60045 USA

    LAB-1087-2.0

    Revised: 03/2019

  • PRINCIPAL DISPLAY PANEL - 50 mL Bag Label

    50 mL
    NDC 0409-6730-11

    MAGNESIUM SULFATE
    IN WATER FOR INJECTION
    4 g/50 mL (80 mg/mL)

    4g
    TOTAL

    EACH 50 mL CONTAINS MAGNESIUM SULFATE
    HEPTAHYDRATE 4 g (EQUIVALENT TO 32.5 mEq
    MAGNESIUM) IN WATER FOR INJECTION. MAY
    CONTAIN SULFURIC ACID AND/OR SODIUM
    HYDROXIDE FOR pH ADJUSTMENT.
    pH 4.5 (3.5 to 6.5) 649 mOsmol/LITER (CALC.)
    SINGLE-DOSE CONTAINER. DISCARD UNUSED
    PORTION. FOR INTRAVENOUS USE.
    RECOMMENDED DOSAGE: SEE PRESCRIBING
    INFORMATION. STERILE, NONPYROGENIC. USE
    ONLY IF SOLUTION IS CLEAR AND CONTAINER IS
    UNDAMAGED. MUST NOT BE USED IN SERIES
    CONNECTIONS.

    Rx ONLY

    IM-5199

    3
    V
    CONTAINS DEHP

    Hospira

    DISTRIBUTED BY
    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    PRINCIPAL DISPLAY PANEL - 50 mL Bag Label
  • PRINCIPAL DISPLAY PANEL - 50 mL Bag Pouch Label

    50 mL
    TO OPEN – TEAR AT NOTCH
    NDC 0409-6730-11

    MAGNESIUM SULFATE
    IN WATER FOR INJECTION

    4 g/50 mL (80 mg/mL)

    4g
    TOTAL

    Each 50 mL contains magnesium sulfate heptahydrate 4 g (equivalent to 32.5 mEq
    magnesium) in water for injection. May contain sulfuric acid and/or sodium hydroxide
    for pH adjustment.

    649 mOsmol/Liter (CALC.)
    pH 4.5 (3.5 to 6.5)

    DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL
    ROUTE.

    Single-dose container. For intravenous use. Recommended dosage: See prescribing
    information. Sterile, nonpyrogenic. Use only if solution is clear. After removing the
    overwrap, check for minute leaks by squeezing container firmly. If leaks are found,
    discard unit as sterility may be impaired. Must not be used in series connections.
    The overwrap is a moisture barrier. Do not remove unit from overwrap until ready for
    use. Use unit promptly when pouch is opened. Store at 20 to 25°C (68 to 77°F). [See USP
    Controlled Room Temperature.] Protect from freezing. See prescribing information.
    Not Made With Natural Rubber Latex.

    Rx only

    7
    OTHER

    Distributed by
    Hospira, Inc., Lake Forest, IL 60045 USA

    F WR-1551

    Hospira

    PRINCIPAL DISPLAY PANEL - 50 mL Bag Pouch Label
  • PRINCIPAL DISPLAY PANEL - 100 mL Bag Label

    100 mL
    NDC 0409-6729-41

    MAGNESIUM SULFATE
    IN WATER FOR INJECTION

    4 g/100 mL (40 mg/mL)

    4g
    TOTAL

    EACH 100 mL CONTAINS MAGNESIUM SULFATE
    HEPTAHYDRATE 4 g (EQUIVALENT TO 32.5 mEq
    MAGNESIUM) IN WATER FOR INJECTION. MAY
    CONTAIN SULFURIC ACID AND/OR SODIUM
    HYDROXIDE FOR pH ADJUSTMENT.
    pH 4.5 (3.5 to 6.5) 325 mOsmol/LITER (CALC.)
    SINGLE-DOSE CONTAINER. DISCARD UNUSED
    PORTION. FOR INTRAVENOUS USE.
    RECOMMENDED DOSAGE: SEE PRESCRIBING
    INFORMATION. STERILE, NONPYROGENIC. USE
    ONLY IF SOLUTION IS CLEAR AND CONTAINER IS
    UNDAMAGED. MUST NOT BE USED IN SERIES
    CONNECTIONS.

    Rx ONLY

    IM-5198

    3
    V
    CONTAINS DEHP

    Hospira

    DISTRIBUTED BY
    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    PRINCIPAL DISPLAY PANEL - 100 mL Bag Label
  • PRINCIPAL DISPLAY PANEL - 100 mL Bag Pouch Label

    100 mL
    TO OPEN – TEAR AT NOTCH
    NDC 0409-6729-41

    MAGNESIUM SULFATE
    IN WATER FOR INJECTION

    4 g/100 mL (40 mg/mL)

    4g
    TOTAL

    Each 100 mL contains magnesium sulfate heptahydrate 4 g (equivalent to 32.5 mEq
    magnesium) in water for injection. May contain sulfuric acid and/or sodium hydroxide
    for pH adjustment.

    325 mOsmol/Liter (CALC.)
    pH 4.5 (3.5 to 6.5)

    DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL
    ROUTE.

    Single-dose container. For intravenous use. Recommended dosage: See prescribing
    information. Sterile, nonpyrogenic. Use only if solution is clear. After removing the
    overwrap, check for minute leaks by squeezing container firmly. If leaks are found,
    discard unit as sterility may be impaired. Must not be used in series connections.
    The overwrap is a moisture barrier. Do not remove unit from overwrap until ready for
    use. Use unit promptly when pouch is opened. Store at 20 to 25°C (68 to 77°F). [See USP
    Controlled Room Temperature.] Avoid excessive heat. Protect from freezing. See
    prescribing information.
    Not Made With Natural Rubber Latex.

    Rx only

    7
    OTHER

    Distributed by
    Hospira, Inc., Lake Forest, IL 60045 USA

    F WR-1550

    Hospira

    PRINCIPAL DISPLAY PANEL - 100 mL Bag Pouch Label
  • PRINCIPAL DISPLAY PANEL - 500 mL Bag Label

    500 mL
    NDC 0409-6729-21

    20 g
    TOTAL

    MAGNESIUM
    SULFATE

    IN WATER FOR INJECTION
    20 g/500 mL (40 mg/mL)

    EACH 100 mL CONTAINS MAGNESIUM SULFATE
    HEPTAHYDRATE 4 g (EQUIVALENT TO 32.5 mEq
    MAGNESIUM) IN WATER FOR INJECTION. MAY CONTAIN
    SULFURIC ACID AND/OR SODIUM HYDROXIDE FOR pH
    ADJUSTMENT.

    pH 4.5 (3.5 to 6.5)
    325 mOsmol/LlTER (CALC.)

    SINGLE-DOSE CONTAINER. DISCARD UNUSED PORTION.
    FOR INTRAVENOUS USE. RECOMMENDED DOSAGE: SEE
    PRESCRIBING INFORMATION. STERILE, NONPYROGENIC.
    USE ONLY IF SOLUTION IS CLEAR AND CONTAINER IS
    UNDAMAGED. MUST NOT BE USED IN SERIES
    CONNECTIONS.

    Rx ONLY

    3
    V
    CONTAINS DEHP

    Hospira

    IM-5196

    DISTRIBUTED BY
    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    PRINCIPAL DISPLAY PANEL - 500 mL Bag Label
  • PRINCIPAL DISPLAY PANEL - 40 mg/mL Bag Overwrap - 500 mL

    TO OPEN TEAR AT NOTCH

    2
    HDPE

    DO NOT REMOVE FROM OVERWRAP UNTIL READY FOR USE. AFTER REMOVING
    THE OVERWRAP, CHECK FOR MINUTE LEAKS BY SQUEEZING CONTAINER FIRMLY.
    IF LEAKS ARE FOUND, DISCARD SOLUTION AS STERILITY MAY BE IMPAIRED.
    RECOMMENDED STORAGE: ROOM TEMPERATURE (25°C). AVOID EXCESSIVE
    HEAT. PROTECT FROM FREEZING. SEE INSERT.
    98-4321-R14-3/98

    PRINCIPAL DISPLAY PANEL - 40 mg/mL Bag Overwrap - 500 mL
  • PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label

    1000 mL
    NDC 0409-6729-31

    MAGNESIUM
    SULFATE
    IN WATER FOR
    INJECTION

    40 g
    TOTAL

    40 g/1000 mL (40 mg/mL)

    EACH 100 mL CONTAINS MAGNESIUM
    SULFATE HEPTAHYDRATE 4 g (EQUIVALENT
    TO 32.5 mEq MAGNESIUM) IN WATER FOR
    INJECTION. MAY CONTAIN SULFURIC ACID
    AND/OR SODIUM HYDROXIDE FOR pH
    ADJUSTMENT.

    pH 4.5 (3.5 to 6.5)
    325 mOsmol/LITER (CALC.)

    SINGLE-DOSE CONTAINER. DISCARD
    UNUSED PORTION. FOR INTRAVENOUS
    USE. RECOMMENDED DOSAGE: SEE
    PRESCRIBING INFORMATION. STERILE,
    NONPYROGENIC. USE ONLY IF SOLUTION
    IS CLEAR AND CONTAINER IS
    UNDAMAGED. MUST NOT BE USED IN
    SERIES CONNECTIONS.

    Rx ONLY

    3
    V
    CONTAINS DEHP

    DISTRIBUTED BY
    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    IM-5197

    Hospira

    PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label
  • PRINCIPAL DISPLAY PANEL - 40 mg/mL Bag Overwrap - 1000 mL

    TO OPEN TEAR AT NOTCH

    2
    HDPE

    DO NOT REMOVE FROM OVERWRAP UNTIL READY FOR USE. AFTER REMOVING
    THE OVERWRAP, CHECK FOR MINUTE LEAKS BY SQUEEZING CONTAINER FIRMLY.
    IF LEAKS ARE FOUND, DISCARD SOLUTION AS STERILITY MAY BE IMPAIRED.
    RECOMMENDED STORAGE: ROOM TEMPERATURE (25°C). AVOID EXCESSIVE
    HEAT. PROTECT FROM FREEZING. SEE INSERT.
    98-4321-R14-3/98

    PRINCIPAL DISPLAY PANEL - 40 mg/mL Bag Overwrap - 1000 mL
  • PRINCIPAL DISPLAY PANEL - 2 g/50 mL Bag Label

    50 mL
    NDC 0409-6729-11

    MAGNESIUM SULFATE
    IN WATER FOR INJECTION

    2g
    TOTAL

    2 g/50 mL (40 mg/mL)

    EACH 50 mL CONTAINS MAGNESIUM SULFATE
    HEPTAHYDRATE 2 g (EQUIVALENT TO 16.25 mEq
    MAGNESIUM) IN WATER FOR INJECTION. MAY
    CONTAIN SULFURIC ACID AND/OR SODIUM
    HYDROXIDE FOR pH ADJUSTMENT.

    pH 4.5 (3.5 to 6.5) 325 mOsmol/LITER (CALC.)

    SINGLE-DOSE CONTAINER. DISCARD UNUSED
    PORTION. FOR INTRAVENOUS USE.
    RECOMMENDED DOSAGE: SEE PRESCRIBING
    INFORMATION. STERILE, NONPYROGENIC. USE
    ONLY IF SOLUTION IS CLEAR AND CONTAINER IS
    UNDAMAGED. MUST NOT BE USED IN SERIES
    CONNECTIONS.

    Rx ONLY

    3
    V
    CONTAINS DEHP

    Hospira

    IM-5195

    DISTRIBUTED BY
    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    PRINCIPAL DISPLAY PANEL - 2 g/50 mL Bag Label
  • PRINCIPAL DISPLAY PANEL - 2 g/50 mL Bag Pouch Label

    50 mL
    TO OPEN – TEAR AT NOTCH
    NDC 0409-6729-11

    MAGNESIUM SULFATE
    IN WATER FOR INJECTION

    2 g
    TOTAL

    2 g/50 mL (40 mg/mL)

    Each 50 mL contains magnesium sulfate heptahydrate 2 g (equivalent to 16.25 mEq
    magnesium) in water for injection. May contain sulfuric acid and/or sodium hydroxide
    for pH adjustment.

    325 mOsmol/Liter (CALC.)
    pH 4.5 (3.5 to 6.5)

    DO NOT ADD SUPPLEMENTARY MEDICATION. WHENEVER POSSIBLE USE CENTRAL
    ROUTE.

    Single-dose container. For intravenous use. Recommended dosage: See prescribing
    information. Sterile, nonpyrogenic. Use only if solution is clear. After removing the
    overwrap, check for minute leaks by squeezing container firmly. If leaks are found,
    discard unit as sterility may be impaired. Must not be used in series connections.
    The overwrap is a moisture barrier. Do not remove unit from overwrap until ready for
    use. Use unit promptly when pouch is opened. Store at 20 to 25°C (68 to 77°F). [See USP
    Controlled Room Temperature.] Protect from freezing. See prescribing information. Not
    Made With Natural Rubber Latex

    Rx only

    7
    OTHER

    Distributed by
    Hospira, Inc., Lake Forest, IL 60045 USA

    F WR-1549

    Hospira

    PRINCIPAL DISPLAY PANEL - 2 g/50 mL Bag Pouch Label
  • INGREDIENTS AND APPEARANCE
    MAGNESIUM SULFATE IN WATER 
    magnesium sulfate in water injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0409-6730
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM SULFATE HEPTAHYDRATE80 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SULFURIC ACID (UNII: O40UQP6WCF)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0409-6730-1324 in 1 CASE03/31/2006
    11 in 1 POUCH
    1NDC:0409-6730-1150 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02030903/31/2006
    MAGNESIUM SULFATE IN WATER 
    magnesium sulfate in water injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0409-6729
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM SULFATE HEPTAHYDRATE40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SULFURIC ACID (UNII: O40UQP6WCF)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0409-6729-2324 in 1 CASE10/13/2005
    11 in 1 POUCH
    1NDC:0409-6729-41100 mL in 1 BAG; Type 0: Not a Combination Product
    2NDC:0409-6729-0324 in 1 CASE08/22/2005
    21 in 1 POUCH
    2NDC:0409-6729-21500 mL in 1 BAG; Type 0: Not a Combination Product
    3NDC:0409-6729-0912 in 1 CASE09/28/2005
    31 in 1 POUCH
    3NDC:0409-6729-311000 mL in 1 BAG; Type 0: Not a Combination Product
    4NDC:0409-6729-2424 in 1 CASE11/21/2006
    41 in 1 POUCH
    4NDC:0409-6729-1150 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02030908/22/2005
    Labeler - Hospira, Inc. (141588017)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hospira, Inc.093132819ANALYSIS(0409-6729, 0409-6730) , LABEL(0409-6729, 0409-6730) , MANUFACTURE(0409-6729, 0409-6730) , PACK(0409-6729, 0409-6730)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hospira, Inc.827731089ANALYSIS(0409-6729, 0409-6730)