Osmitrol

Product NDC
0338-0353
11-digit product format
003380353
Labeler code
0338
Product ID
0338-0353_3911fd42-2b73-4509-9c4c-92ceba4e6d34
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mannitol
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Baxter Healthcare Company
Application
NDA013684
Marketing category
NDA
Marketing start
1964-06-08
Substance
MANNITOL
Active strength
10 g/100mL
Pharmacologic classes
Increased Diuresis [PE], Osmotic Activity [MoA], Osmotic Diuretic [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Orange Book products#

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N013684-001OSMITROL 5% IN WATERMANNITOL5GM/100MLINJECTABLE / INJECTIONAPApproved before 1982
N013684-002OSMITROL 10% IN WATERMANNITOL10GM/100MLINJECTABLE / INJECTIONAPApproved before 1982
N013684-003OSMITROL 20% IN WATERMANNITOL20GM/100MLINJECTABLE / INJECTIONAPApproved before 1982
N013684-004OSMITROL 15% IN WATERMANNITOL15GM/100MLINJECTABLE / INJECTIONAPApproved before 1982
N013684-005OSMITROL 5% IN WATER IN PLASTIC CONTAINERMANNITOL5GM/100MLINJECTABLE / INJECTIONAPApproved before 1982
N013684-006OSMITROL 10% IN WATER IN PLASTIC CONTAINERMANNITOL10GM/100MLINJECTABLE / INJECTIONAPApproved before 1982
N013684-007OSMITROL 20% IN WATER IN PLASTIC CONTAINERMANNITOL20GM/100MLINJECTABLE / INJECTIONAPRLD, RS, Approved before 1982
N013684-008OSMITROL 15% IN WATER IN PLASTIC CONTAINERMANNITOL15GM/100MLINJECTABLE / INJECTIONAPApproved before 1982

Therapeutic equivalence codes#

Application-product, TE code table
Application-productTE code
N013684-001AP
N013684-002AP
N013684-003AP
N013684-004AP
N013684-005AP
N013684-006AP
N013684-007AP
N013684-008AP

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
OsmitrolMANNITOLBaxter Healthcare Company0d914965-7001-45cb-ba51-d7c5964b05bc2025-08-26Warnings, Adverse reactionsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings and cautions

5 WARNINGS AND PRECAUTIONS • Hypersensitivity Reactions, including anaphylaxis : Stop infusion immediately if hypersensitivity reactions develop. ( 5.1 ) • Renal Complications Including Renal Failure : Risk factors include pre-existing renal failure, concomitant use of nephrotoxic drugs or other diuretics. Avoid use of nephrotoxic drugs. Discontinue OSMITROL if renal function worsens. ( 5.2 , 8.6 ) • Central Nervous System (CNS) Toxicity : Confusion, lethargy and coma may occur during or after infusion. Concomitant neurotoxic drugs may potentiate toxicity. Avoid use of neurotoxic drugs. Discontinue OSMITROL if CNS toxicity develops. ( 5.3 ) • Fluid and Electrolyte Imbalances, Hyperosmolarity : Hypervolemia may exacerbate congestive heart failure, hyponatremia can lead to encephalopathy; hypo/hyperkalemia can result in cardiac adverse reactions in sensitive patients. Discontinue OSMITROL if fluid and/or electrolyte imbalances occur. ( 5.4 ) • Monitoring/Laboratory Tests : Monitor fluid and electrolytes, serum osmolarity and renal, cardiac and pulmonary function. Discontinue if toxicity develops. ( 5.5 ) • Infusion Site Reactions : May include irritation and inflammation, as well as severe reactions (compartment syndrome) when associated with extravasation. ( 5.6 ) • Interference with Laboratory Tests : High concentrations of mannitol may cause false low results of inorganic phosphorus blood concentrations. Mannitol may produce false positive results for blood ethylene glycol. ( 5.7 , 7.6 ) 5.1 Hypersensitivity Reactions Serious hypersensitivity reactions, including anaphylaxis, hypotension and dyspnea resulting in cardiac arrest and death have been reported with OSMITROL [see Adverse Reactions (6) ]. Stop the infusion immediately if signs or symptoms of a suspected hypersensitivity reaction develop. Initiate appropriate therapeutic countermeasures as clinically indicated. 5.2 Renal Complications Including Renal Failure Renal complications, including irreversible renal failure have been reported in patients receiving mannitol. Reversible, oliguric acute kidney injury (AKI) has occurred in patients with normal pretreatment renal function who received large intravenous doses of mannitol. Although the osmotic nephrosis associated with mannitol administration is in principle reversible, osmotic nephrosis in general is known to potentially proceed chronic or eve...

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

adverse reactions

6 ADVERSE REACTIONS The following adverse reactions from voluntary reports or clinical studies have been reported with OSMITROL. Because many of these reactions were reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure. • Hypersensitivity reactions : cardiac arrest, anaphylaxis, hypotension, dyspnea, hypertension, pyrexia, chills, sweating, cough, musculoskeletal stiffness, myalgia, urticarial/rash, pruritus, generalized pain, discomfort, nausea, vomiting, and headache. [see Warnings and Precautions (5.1) ] • Renal Failure : acute kidney injury, osmotic nephrosis, azotemia, anuria, hematuria, oliguria, polyuria [see Warnings and Precautions (5.2) ] • CNS Toxicity : coma, seizures, confusion, lethargy; rebound increase in intracranial pressure; dizziness [see Warnings and Precautions (5.3) ] • Fluid and Electrolyte Imbalances : hypovolemia, hypervolemia, peripheral edema, dehydration, hyponatremia, hypernatremia, hyperkalemia, hypokalemia; metabolic acidosis [see Warnings and Precautions (5.4) ] • Infusion Site Reactions : phlebitis, inflammation, pain, rash, erythema, pruritus; compartment syndrome and swelling associated with extravasation [see Warnings and Precautions (5.6) ] • Cardiac and Respiratory Disorders : congestive cardiac failure, pulmonary edema, palpitations • Gastrointestinal Disorders : thirst, dry mouth • General Disorders : asthenia, malaise The most common adverse reactions are hypersensitivity reactions, renal failure, CNS toxicity, hypo/hypervolemia, hypo/hypernatremia, hypo/hyperkalemia, and infusion site reactions. ( 6 ) To report SUSPECTED ADVERSE REACTIONS, contact Baxter Healthcare at 1-866-888-2472 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Additional Listing Data#

Finished product
Yes
Brand name base
Osmitrol
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MANNITOL10 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii3OWL53L36A
Rxcui206536, 1791395, 1791403, 1791404, 1791408, 1791409

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a62a50ac-1535-4461-9768-8ae703e2e9fbProduct name120210525
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508
bc07ef78-e82d-0c19-31f4-31f263780582Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0338-0353-03Osmitrol500 mL in 1 BAGINJECTION, SOLUTION50016

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0338-0353-03ML - Milliliter0338-03532a2bdc99-cc36-48e6-a813-fceebf32763f12012-07-24
0338-0353-04ML - Milliliter0338-03530d95cd58-3613-4571-9e37-713a20d33be912012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0338-0353OSMITROL (MANNITOL) INJECTION, SOLUTION [BAXTER HEALTHCARE COMPANY]14Current NDC, Legacy NDC, 1 package rows20250519_0d914965-7001-45cb-ba51-d7c5964b05bc.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1791395mannitol 10 % in 500 ML InjectionPSN0d914965-7001-45cb-ba51-d7c5964b05bc16
1791403mannitol 20 % in 250 ML InjectionPSN0d914965-7001-45cb-ba51-d7c5964b05bc16
1791408mannitol 20 % in 500 ML InjectionPSN0d914965-7001-45cb-ba51-d7c5964b05bc16
206536OSMITROL 10 % in 500 ML InjectionPSN0d914965-7001-45cb-ba51-d7c5964b05bc16
1791404OSMITROL 20 % in 250 ML InjectionPSN0d914965-7001-45cb-ba51-d7c5964b05bc16
1791409OSMITROL 20 % in 500 ML InjectionPSN0d914965-7001-45cb-ba51-d7c5964b05bc16
1791404250 ML mannitol 200 MG/ML Injection [Osmitrol]SBD0d914965-7001-45cb-ba51-d7c5964b05bc16
206536500 ML mannitol 100 MG/ML Injection [Osmitrol]SBD0d914965-7001-45cb-ba51-d7c5964b05bc16
1791409500 ML mannitol 200 MG/ML Injection [Osmitrol]SBD0d914965-7001-45cb-ba51-d7c5964b05bc16
1791403250 ML mannitol 200 MG/ML InjectionSCD0d914965-7001-45cb-ba51-d7c5964b05bc16
1791395500 ML mannitol 100 MG/ML InjectionSCD0d914965-7001-45cb-ba51-d7c5964b05bc16
1791408500 ML mannitol 200 MG/ML InjectionSCD0d914965-7001-45cb-ba51-d7c5964b05bc16
1791404250 ML Osmitrol 200 MG/ML InjectionSY0d914965-7001-45cb-ba51-d7c5964b05bc16
206536500 ML Osmitrol 100 MG/ML InjectionSY0d914965-7001-45cb-ba51-d7c5964b05bc16
1791409500 ML Osmitrol 200 MG/ML InjectionSY0d914965-7001-45cb-ba51-d7c5964b05bc16
1791395mannitol 10 % per 500 ML InjectionSY0d914965-7001-45cb-ba51-d7c5964b05bc16
1791403mannitol 20 % per 250 ML InjectionSY0d914965-7001-45cb-ba51-d7c5964b05bc16
1791408mannitol 20 % per 500 ML InjectionSY0d914965-7001-45cb-ba51-d7c5964b05bc16
206536Osmitrol 10 % per 500 ML InjectionSY0d914965-7001-45cb-ba51-d7c5964b05bc16
1791404Osmitrol 20 % per 250 ML InjectionSY0d914965-7001-45cb-ba51-d7c5964b05bc16
1791409Osmitrol 20 % per 500 ML InjectionSY0d914965-7001-45cb-ba51-d7c5964b05bc16

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0338-0353-0300338035303500 mL in 1 BAG (0338-0353-03) 500 ml1964-06-080000-00-00NoNoCurrent