Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate
Magnesium sulfate, potassium sulfate, and sodium sulfate is an osmotic laxative oral solution used to cleanse the colon before a colonoscopy.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 12 clinical label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
📖 Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate: Patient Information Guide
A plain-language walkthrough of Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate — what it treats, how it works, how it’s taken, side effects, warnings and interactions. Tap any section to expand it.
🎯What it's used for▾
This combination of sulfate salts is an osmotic laxative oral solution used exclusively to clean out the colon before a colonoscopy.
- Approved for colonoscopy bowel prep in adult patients across all labeled oral solution products
- SUPREP Bowel Prep Kit is approved for colonoscopy prep in adults and pediatric patients 12 years of age and older
- Potassium Sulfate and Magnesium Sulfate Oral solution is approved for colonoscopy prep in adults and pediatric patients 12 years of age and older
- Several other labeled oral solution products are approved for adult use only — pediatric approval is product-specific and not universal across all formulations
⚙️How it works▾
This prep contains sulfate salts (sodium sulfate, potassium sulfate, and magnesium sulfate) that are poorly absorbed by the gut. Because they stay inside the intestine, they draw water inward through osmosis — the natural movement of water toward areas of higher concentration. This retained water flushes the colon clear, producing the bowel movements needed to prepare for colonoscopy.
💊How it's taken▾
This solution is taken by mouth using a split-dose, two-day regimen — one dose the evening before the colonoscopy and one dose the morning of the procedure. Each dose must be diluted with water before drinking, and extra water must be consumed after each dose to stay hydrated. Stop all fluids at least 2 hours before the scheduled colonoscopy. Always follow your prescriber's exact instructions and the directions in your kit — do not take both doses in a single evening, as this is not a recommended regimen and is associated with more side effects.
- Must dilute in water before ingesting — never take undiluted
- Drink additional water after each dose as directed
- Take other oral medications at least 1 hour before starting each dose
- Stop fluids at least 2 hours before colonoscopy
🤒Side effects — in detail▾
Most people will experience some GI discomfort — that is expected with any bowel prep. Common side effects include:
- Overall discomfort
- Abdominal bloating or distension
- Abdominal pain or cramping
- Nausea
- Vomiting
More serious reactions to watch for include signs of dehydration, irregular heartbeat, seizures, or a severe allergic reaction (trouble breathing, throat swelling, hives). Seek medical help right away if any of these occur.
⚠️Warnings & precautions▾
- Fluid and electrolyte imbalance: The biggest risk. Losing too much water or minerals can cause serious heart rhythm problems, seizures, or kidney injury. Drink plenty of water as directed and get lab tests if your doctor recommends it.
- Cardiac arrhythmias (irregular heartbeat): Rare but serious. People with a history of prolonged QT interval, heart failure, recent heart attack, unstable angina, or cardiomyopathy should discuss the risks with their doctor before use. An ECG (heart tracing) may be recommended before and after the procedure.
- Seizures: Have been reported, mostly linked to electrolyte abnormalities. Extra caution is needed for people with a history of seizures, those withdrawing from alcohol or benzodiazepines, or those taking medications that lower the seizure threshold.
- Kidney injury: People with kidney disease or those taking diuretics, ACE inhibitors, ARBs, or NSAIDs are at higher risk. Lab testing before and after may be needed.
- Severe allergic reactions (anaphylaxis): Rare but possible. Seek emergency care immediately for breathing difficulty, facial swelling, or hives.
- Colonic ulceration or ischemic colitis (reduced blood flow to the colon): Risk increases if stimulant laxatives are used at the same time — avoid them.
- Aspiration risk: People with swallowing problems or a weak gag reflex should be monitored during administration.
- Gout flares: This prep can temporarily raise uric acid levels, which may trigger a gout attack in susceptible people.
🔀What it interacts with▾
This bowel prep can interact with several types of medications — tell your doctor and pharmacist about everything you take before using it.
- Diuretics, ACE inhibitors, ARBs, NSAIDs: Increase risk of kidney injury and electrolyte problems when combined with this prep
- Tricyclic antidepressants and other drugs that lower seizure threshold: Raise the risk of seizures if electrolytes become abnormal during prep
- Stimulant laxatives (bisacodyl, sodium picosulfate): Avoid — combining these with this prep raises the risk of colonic ulcerations and ischemic colitis
- All oral medications: Take at least 1 hour before starting each dose, as this prep can reduce drug absorption
- Tetracycline and fluoroquinolone antibiotics, iron, digoxin, chlorpromazine, penicillamine: Take at least 2 hours before and no less than 6 hours after each dose — magnesium in the prep can bind to these drugs and reduce their effectiveness
- Medications that prolong the QT interval (affect heart rhythm): Use with caution; electrolyte shifts during prep may worsen the risk
This is not a complete list of interactions. Always talk with your doctor or pharmacist before starting, stopping, or changing any medication.
📋Before taking it▾
- Do not use if you have a bowel blockage (obstruction or ileus), bowel perforation, gastric retention, or toxic colitis or megacolon
- Do not use if you have a known allergy to any ingredient in the solution
- Kidney disease: Use with caution; may need lab tests before and after the prep
- Heart disease or irregular heart rhythm: Discuss risks with your doctor; an ECG may be recommended
- History of seizures: Use with extra caution; inform your doctor
- Gout or uric acid disorders: Prep can temporarily raise uric acid — discuss with your doctor beforehand
- Severe active ulcerative colitis: Use with caution
- Swallowing difficulties or impaired gag reflex: Should be monitored during use due to aspiration risk
- Children under 12: Safety and effectiveness have not been established
- Older adults: More likely to be sensitive to fluid and electrolyte changes — monitor carefully
- Pregnancy: No human data available on safety — discuss with your doctor
- Breastfeeding: No data available on whether the drug passes into breast milk — discuss with your doctor
🚑If you take too much▾
Taking more than the recommended amount of this prep can lead to severe electrolyte disturbances, dehydration, and low blood volume (hypovolemia). These can cause serious heart, kidney, and neurological problems. If an overdose is suspected, monitor for fluid and electrolyte imbalances and seek medical treatment promptly.
🔬Pharmacokinetics — how your body processes it▾
After taking this solution, sulfate levels in the blood peak at about 17 hours after the first dose and around 5 hours after the second dose. Sulfate then clears from the body with a half-life of about 8.5 hours — meaning the body eliminates roughly half of it every 8.5 hours. The primary route of elimination is through the stool (fecal excretion). In people with moderate kidney impairment, sulfate exposure is somewhat higher than in people with normal kidney function, but these differences are not considered clinically meaningful. Liver impairment does not appear to significantly affect how the body handles sulfate from this prep.
📦How to store it▾
Store at 20°C to 25°C (68°F to 77°F). Keep out of reach of children.
📄 Written from Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Every point is grounded in that labeling — nothing is invented. How we use AI →
🩺 Pharmacist Counseling Corner
Quick, plain-English answers to the questions patients ask most about Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate — the kind of thing our pharmacy team would talk through with you at the counter.
What exactly does this prep do, and why do I have to drink so much water with it? ▾
Can I take my regular medications while I'm doing the prep? ▾
What side effects should I expect, and which ones mean I need to call for help? ▾
I have kidney disease — is it safe for me to use this prep? ▾
Is it safe to take this prep if I'm pregnant or breastfeeding? ▾
Why do I take this in two doses instead of all at once the night before? ▾
Is Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate available over the counter? ▾
When was Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate first available? ▾
Who makes Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate? ▾
💬 Answers drafted from Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Grounded in that labeling — nothing is made up. How we use AI →
🧰 Keep exploring
💊 How Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate comes
Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate is available in 1 form. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Oral solution
How this form is used
- Used to cleanse the colon in preparation for colonoscopy in adult patients
- SUPREP Bowel Prep Kit is approved for colonoscopy prep in adults and pediatric patients 12 years of age and older
- Potassium Sulfate and Magnesium Sulfate Oral solution is approved for colonoscopy prep in adults and pediatric patients 12 years of age and older
- Must be diluted with water before drinking — do not swallow undiluted
- Taken as a split-dose (two-day) regimen: first dose the evening before colonoscopy, second dose the morning of the procedure
- SUPREP Bowel Prep Kit: after each dose, additional water must be consumed as directed; stop all fluids at least 2 hours before the colonoscopy
- Take all other oral medications at least 1 hour before starting each dose to prevent reduced absorption
Show 5 more strengths Show fewer strengths
📊 Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate across the U.S. market
How Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
📈 How widely Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate is used
A general measure of how commonly Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate prescribed? Of the 1,596 medications we measure, Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate ranks #458 by Medicaid prescriptions — more than 71% of them.
Utilization by Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
magnesium sulfate 0.0277 MEQ/ML / potassium sulfate 0.0374 MEQ/ML / sodium sulfate 0.257 MEQ/ML Oral Solution
Summed across the 4 of 10 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1120068
Other Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate products — combination packs and listings not yet matched to a specific clinical product (kept visible so every prescription is accounted for)
Summed across the 5 of 14 listed NDC products with Medicaid activity.
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 9 of 24 listed Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate NDCs with Medicaid activity.
🔍 Compare Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate products
A representative set of FDA-listed product records for Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Oral solution | ||||
| SODIUM SULFATE 13.13 g/133.1 mL; POTASSIUM SULFATE 2.35 g/133.1 mL; MAGNESIUM SULFATE, UNSPECIFIED FORM 1.2 g/133.1 mL | Oral | Affordable Pharmaceuticals, LLC | NDA | View NDC → |
| SODIUM SULFATE 17.5 g/mL; POTASSIUM SULFATE 3.13 g/mL; MAGNESIUM SULFATE, UNSPECIFIED FORM 1.6 g/mL | Oral | Affordable Pharmaceuticals, LLC | NDA | View NDC → |
| 1.2; 2.35; 13.13 g/133.1 mL; g/133.1 mL; g/133.1 mL | Oral | Affordable Pharmaceuticals, LLC | NDA | View NDC → |
| 1.6; 3.13; 17.5 g/mL; g/mL; g/mL | Oral | Affordable Pharmaceuticals, LLC | NDA | View NDC → |
| SODIUM SULFATE 1.6 g/177 mL; POTASSIUM SULFATE 3.13 g/177 mL; MAGNESIUM SULFATE, UNSPECIFIED FORM 17.5 g/177 mL | Oral | Ascend Laboratories, LLC | ANDA | View NDC → |
| SODIUM SULFATE 17.5 g/177 mL; POTASSIUM SULFATE 3.13 g/177 mL; MAGNESIUM SULFATE, UNSPECIFIED FORM 1.6 g/177 mL | Oral | Ascend Laboratories, LLC | ANDA | View NDC → |
| SODIUM SULFATE 13.13 g/133.1 mL; POTASSIUM SULFATE 2.35 g/133.1 mL; MAGNESIUM SULFATE, UNSPECIFIED FORM 1.2 g/133.1 mL | Oral | Azurity Pharmaceuticals, Inc. | NDA | View NDC → |
| SODIUM SULFATE 17.5 g/mL; POTASSIUM SULFATE 3.13 g/mL; MAGNESIUM SULFATE, UNSPECIFIED FORM 1.6 g/mL | Oral | Azurity Pharmaceuticals, Inc. | NDA | View NDC → |
| MAGNESIUM SULFATE ANHYDROUS 1.6 g/177 mL; POTASSIUM SULFATE 3.13 g/177 mL; SODIUM SULFATE 17.5 g/177 mL | Oral | Bionpharma Inc., | ANDA | View NDC → |
| SODIUM SULFATE 17.5 g/177 mL; POTASSIUM SULFATE 3.13 g/177 mL; MAGNESIUM SULFATE ANHYDROUS 1.6 g/177 mL | Oral | Bionpharma Inc., | ANDA | View NDC → |
| SODIUM SULFATE 13.13 g/133.1 mL; POTASSIUM SULFATE 2.35 g/133.1 mL; MAGNESIUM SULFATE, UNSPECIFIED FORM 1.2 g/133.1 mL | Oral | Braintree Laboratories, Inc. | NDA | View NDC → |
| SODIUM SULFATE 17.5 g/mL; POTASSIUM SULFATE 3.13 g/mL; MAGNESIUM SULFATE, UNSPECIFIED FORM 1.6 g/mL | Oral | Braintree Laboratories, Inc. | NDA | View NDC → |
| 1.2; 2.35; 13.13 g/133.1 mL; g/133.1 mL; g/133.1 mL | Oral | Braintree Laboratories, Inc. | NDA | View NDC → |
| 1.6; 3.13; 17.5 g/mL; g/mL; g/mL | Oral | Braintree Laboratories, Inc. | NDA | View NDC → |
| SODIUM SULFATE 17.5 g/177 mL; POTASSIUM SULFATE 3.13 g/177 mL; MAGNESIUM SULFATE 1.6 g/177 mL | Oral | Camber Pharmaceuticals, Inc. | ANDA | View NDC → |
| SODIUM SULFATE 17.5 g/177 mL; POTASSIUM SULFATE 3.13 g/177 mL; MAGNESIUM SULFATE ANHYDROUS 1.6 g/177 mL | Oral | Lupin Pharmaceuticals, Inc. | ANDA | View NDC → |
| 1.6; 3.13; 17.5 g/177 mL; g/177 mL; g/177 mL | Oral | Lupin Pharmaceuticals, Inc. | ANDA | View NDC → |
| SODIUM SULFATE 17.5 g/177 mL; POTASSIUM SULFATE 3.13 g/177 mL; MAGNESIUM SULFATE 1.6 g/177 mL | Oral | NorthStar RxLLC | ANDA | View NDC → |
| SODIUM SULFATE 17.5 g/177 mL; POTASSIUM SULFATE 3.13 g/177 mL; MAGNESIUM SULFATE ANHYDROUS 1.6 g/177 mL | Oral | Novel Laboratories, Inc. | ANDA | View NDC → |
| SODIUM SULFATE 17.5 g/177 mL; POTASSIUM SULFATE 3.13 g/177 mL; MAGNESIUM SULFATE, UNSPECIFIED FORM 1.6 g/177 mL | Oral | Strides Pharma Science Limited | ANDA | View NDC → |
| SODIUM SULFATE ANHYDROUS 17.5 g/177 mL; POTASSIUM SULFATE 3.13 g/177 mL; MAGNESIUM SULFATE, UNSPECIFIED FORM 1.6 g/177 mL | Oral | Sun Pharmaceutical Industries, Inc. | ANDA | View NDC → |
| SODIUM SULFATE 13.13 g/133.1 mL; POTASSIUM SULFATE 2.35 g/133.1 mL; MAGNESIUM SULFATE, UNSPECIFIED FORM 1.2 g/133.1 mL | Oral | Wilshire Pharmaceuticals, Inc. | NDA | View NDC → |
| SODIUM SULFATE 17.5 g/mL; POTASSIUM SULFATE 3.13 g/mL; MAGNESIUM SULFATE, UNSPECIFIED FORM 1.6 g/mL | Oral | Wilshire Pharmaceuticals, Inc. | NDA | View NDC → |
Showing 23 of 23 products — FDA National Drug Code Directory. See every product, package size and price: browse all 23 Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate NDCs →
📈 What people report — real-world data (FDA FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
🏛️ The road to your pharmacy
How Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
🚨 Recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
Source: openFDA drug enforcement (recall) reports.
📦 Supply & shortage status
Whether Magnesium Sulfate, Potassium Sulfate, and Sodium Sulfate is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
🏷️ Sold under these brand names
🏭 Manufacturers & labelers
🔬 Where this comes from
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How we combine label and product data
HelloPharmacist combines public FDA and NLM records; we don’t author the underlying clinical facts. We identified 12 FDA-filed SPL label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. The representative label is the starting point for the displayed reference monograph; the 12 largest stored in-scope SPL records, which may include that representative, are compared section by section, and the longest available version of each section is retained. Forms, routes, brands, labelers, product-listed strengths, and product-record counts are aggregated separately from ingredient-matched FDA NDC Directory records; package records listed above are associated with the linked SPL; and the normalized concept hierarchy comes from NLM RxNorm.
For canonical ingredient pages, bounded product-attributed indication and administration excerpts may be added to the AI evidence, and the generator is instructed to preserve available product, brand, route, and form qualifiers instead of treating one label as universal. Where a section is identified as AI-written, its plain-language text is generated from bounded label evidence. New draft drug pages remain in the admin review queue before first publication. Braintree Laboratories, Inc. is the representative DailyMed label linked for verification and dates; it is not the sole source used for the page.
This is general education, not medical advice — always consult your doctor or pharmacist about your medications and any medical condition. For the exact wording of the linked representative label, view that label on DailyMed; some displayed composite sections may come from other in-scope SPL labels. Learn how we use AI and our data sources & update cadence.