ionosol mb and dextrose

Generic: dextrose monohydrate, sodium lactate, potassium chloride, magnesium chloride, potassium phosphate, monobasic, and sodium phosphate, monobasic, monohydrate

Labeler: icu medical inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name ionosol mb and dextrose
Generic Name dextrose monohydrate, sodium lactate, potassium chloride, magnesium chloride, potassium phosphate, monobasic, and sodium phosphate, monobasic, monohydrate
Labeler icu medical inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 5 g/100mL, magnesium chloride 30 mg/100mL, monobasic potassium phosphate 15 mg/100mL, potassium chloride 141 mg/100mL, sodium lactate 260 mg/100mL, sodium phosphate, monobasic, monohydrate 25 mg/100mL

Manufacturer
ICU Medical Inc.

Identifiers & Regulatory

Product NDC 0990-7372
Product ID 0990-7372_e8e6f73c-5771-44a4-84b6-6f0ed79c63d2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019513
Listing Expiration 2026-12-31
Marketing Start 2019-07-01

Pharmacologic Class

Classes
calculi dissolution agent [epc] increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] inhibition small intestine fluid/electrolyte absorption [pe] magnesium ion exchange activity [moa] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc] stimulation large intestine fluid/electrolyte secretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09907372
Hyphenated Format 0990-7372

Supplemental Identifiers

RxCUI
800644 800648
UNII
LX22YL083G 02F3473H9O 4J9FJ0HL51 660YQ98I10 TU7HW0W0QT 593YOG76RN

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ionosol mb and dextrose (source: ndc)
Generic Name dextrose monohydrate, sodium lactate, potassium chloride, magnesium chloride, potassium phosphate, monobasic, and sodium phosphate, monobasic, monohydrate (source: ndc)
Application Number NDA019513 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 g/100mL
  • 30 mg/100mL
  • 15 mg/100mL
  • 141 mg/100mL
  • 260 mg/100mL
  • 25 mg/100mL
source: ndc
Packaging
  • 24 POUCH in 1 CASE (0990-7372-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG
  • 24 POUCH in 1 CASE (0990-7372-62) / 1 BAG in 1 POUCH / 250 mL in 1 BAG
source: ndc

Packages (2)

0990-7372-03 24 POUCH in 1 CASE (0990-7372-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG 0990-7372-62 24 POUCH in 1 CASE (0990-7372-62) / 1 BAG in 1 POUCH / 250 mL in 1 BAG

Ingredients (6)

dextrose monohydrate (5 g/100mL) magnesium chloride (30 mg/100mL) monobasic potassium phosphate (15 mg/100mL) potassium chloride (141 mg/100mL) sodium lactate (260 mg/100mL) sodium phosphate, monobasic, monohydrate (25 mg/100mL)

Linked Drug Pages (1)

Ionosol MB and Dextrose ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "e8e6f73c-5771-44a4-84b6-6f0ed79c63d2", "openfda": {"unii": ["LX22YL083G", "02F3473H9O", "4J9FJ0HL51", "660YQ98I10", "TU7HW0W0QT", "593YOG76RN"], "rxcui": ["800644", "800648"], "spl_set_id": ["1b457b1d-0e80-4578-ba6f-dedf513fc962"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 POUCH in 1 CASE (0990-7372-03)  / 1 BAG in 1 POUCH / 500 mL in 1 BAG", "package_ndc": "0990-7372-03", "marketing_start_date": "20200101"}, {"sample": false, "description": "24 POUCH in 1 CASE (0990-7372-62)  / 1 BAG in 1 POUCH / 250 mL in 1 BAG", "package_ndc": "0990-7372-62", "marketing_start_date": "20190701"}], "brand_name": "Ionosol MB and Dextrose", "product_id": "0990-7372_e8e6f73c-5771-44a4-84b6-6f0ed79c63d2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Calculi Dissolution Agent [EPC]", "Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Compounds [CS]", "Potassium Salt [EPC]", "Potassium Salt [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "0990-7372", "generic_name": "DEXTROSE MONOHYDRATE, SODIUM LACTATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, POTASSIUM PHOSPHATE, MONOBASIC, and SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ionosol MB and Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "MAGNESIUM CHLORIDE", "strength": "30 mg/100mL"}, {"name": "MONOBASIC POTASSIUM PHOSPHATE", "strength": "15 mg/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "141 mg/100mL"}, {"name": "SODIUM LACTATE", "strength": "260 mg/100mL"}, {"name": "SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE", "strength": "25 mg/100mL"}], "application_number": "NDA019513", "marketing_category": "NDA", "marketing_start_date": "20190701", "listing_expiration_date": "20261231"}