Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / Sodium Sulfate
A combination of PEG-3350, electrolytes, and ascorbate used as an osmotic laxative to clean the colon before a colonoscopy in adults.
🧬 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 3 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 →
📖 Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / Sodium Sulfate: Patient Information Guide
A plain-language walkthrough of Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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 ingredient combination is the active basis for several prescription colonoscopy prep products, each indicated for the same purpose in adults.
- MoviPrep is indicated to cleanse the colon as a preparation for colonoscopy in adults
- PLENVU is indicated to cleanse the colon as a preparation for colonoscopy in adults
- Polyethylene Glycol-3350, Electrolytes, and Ascorbate for Oral Solution (generic) is indicated to cleanse the colon as a preparation for colonoscopy in adults
⚙️How it works▾
These ingredients work together through an osmotic effect — they are not well absorbed in the gut, so they draw large amounts of water into the colon and hold it there. The resulting surge of fluid produces a strong, watery diarrhea that flushes the bowel clean. PEG-3350, sodium sulfate, sodium ascorbate, and ascorbic acid all contribute to this osmotic pull. Most people experience their first bowel movement within about 1 to 2 hours of starting the preparation.
💊How it's taken▾
These preparations are taken as a reconstituted oral liquid — you mix powder pouches with water before drinking. Two separate doses are always needed for a complete bowel prep. Your prescriber will choose from two dosing schedules:
- Split-dose (Two-Day): First dose the evening before the colonoscopy, second dose the morning of the colonoscopy (roughly 12 hours apart) — this is the preferred method for MoviPrep and the generic, and a standard option for PLENVU
- Same-evening (One-Day Evening-Only): Both doses taken the evening before the colonoscopy, at least 90 minutes apart — an alternative method for MoviPrep and the generic
- One-Day Morning (PLENVU): Both doses taken the morning of the colonoscopy, with at least 2 hours between the start of dose 1 and the start of dose 2
Drink additional clear liquids after each dose, eat only clear liquids from the start of prep until after the colonoscopy, and take all other oral medications at least 1 hour before each dose. Follow your prescriber's specific instructions closely.
🤒Side effects — in detail▾
Most people experience some gastrointestinal discomfort — that's a normal part of how this preparation works.
- Nausea
- Abdominal pain or cramping
- Vomiting
- Bloating or abdominal distension
- Malaise (feeling generally unwell or run-down)
- Anal discomfort
- Thirst
- Dizziness
- Sleep disturbance
Diarrhea is expected and is how the preparation does its job. More serious reactions — including severe allergic reactions, irregular heartbeat, seizures, or signs of kidney injury — are rare but require immediate medical attention.
⚠️Warnings & precautions▾
- Fluid and electrolyte imbalances are the most important risk. Losing too much fluid or having shifts in sodium, potassium, or other minerals can trigger serious heart rhythm problems, seizures, or kidney injury. Drink plenty of fluids and call your doctor if you vomit heavily or feel severely dehydrated.
- Cardiac arrhythmias (irregular heartbeat) have been reported rarely, mainly in people with existing heart conditions or electrolyte problems. Your doctor may order an ECG (heart tracing) before and after the procedure if you are at higher risk.
- Seizures have occurred rarely, linked to electrolyte imbalances. Extra caution is needed if you have a seizure history or take medications that lower the seizure threshold.
- Kidney injury is possible, especially if you have existing kidney disease or take medications that affect kidney function. Stay well hydrated.
- Severe allergic reactions (anaphylaxis), including swelling, trouble breathing, and rash, have been reported. Seek emergency care immediately if these occur.
- Aspiration risk: People with swallowing problems should be monitored while taking the liquid. Never mix with starch-based thickeners — doing so can thin the liquid and increase choking risk.
- Contains phenylalanine — people with phenylketonuria (PKU) must discuss this with their doctor before using.
- Use with extra caution if you have G6PD deficiency, as the ascorbate component may trigger hemolysis (breakdown of red blood cells).
🔀What it interacts with▾
Several medications and substances can interact with this bowel preparation by increasing the risk of electrolyte problems, kidney injury, or other complications.
- Diuretics (water pills): Already affect fluid and electrolyte balance; combining with this prep raises the risk of imbalances further
- ACE inhibitors and ARBs (blood pressure medications): Can worsen kidney stress and electrolyte shifts during the prep
- NSAIDs (like ibuprofen or naproxen): May increase the risk of kidney injury, especially with dehydration
- Tricyclic antidepressants and other medications that lower the seizure threshold: Raise seizure risk when electrolytes are disturbed
- All oral medications: This preparation can reduce how well your body absorbs other drugs — take all oral medications at least 1 hour before starting each dose
- Stimulant laxatives (bisacodyl, sodium picosulfate): Do not use at the same time — increases risk of ulceration or ischemic colitis in the colon
- Starch-based thickeners: Never mix these into the solution — PEG thins starch-thickened liquids and can cause choking or aspiration
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 (GI obstruction), bowel perforation, gastric retention, ileus, or toxic colitis or toxic megacolon — these are contraindications
- Tell your doctor about any allergy to any ingredient, including polyethylene glycol or lemon flavoring components
- Tell your doctor if you have kidney disease or take medications that affect kidney function
- Tell your doctor if you have heart disease, irregular heartbeat, heart failure, recent heart attack, or unstable angina
- Tell your doctor if you have a history of seizures or take medications that lower the seizure threshold
- Tell your doctor if you have G6PD deficiency — the ascorbate content may trigger hemolysis
- Tell your doctor if you have phenylketonuria (PKU) — this preparation contains phenylalanine
- Tell your doctor if you have severe ulcerative colitis or suspected inflammatory bowel disease
- If you have trouble swallowing or an impaired gag reflex, tell your care team — you should be monitored during administration
- Pregnancy: There are no adequate human data on safety; discuss with your doctor
- Breastfeeding: Not enough data is available; discuss risks and benefits with your doctor
- Children: Safety and effectiveness have not been established in pediatric patients
- Older adults: Used safely in clinical trials, but elderly patients are more susceptible to fluid and electrolyte problems and should be monitored closely
🚑If you take too much▾
Taking more than the recommended amount can cause severe electrolyte disturbances — including dangerously low sodium (hyponatremia) or potassium (hypokalemia) — as well as dehydration and low blood volume. In serious cases, this can lead to heart rhythm problems, seizures, or kidney failure.
If overdose is suspected, seek medical attention and treatment will focus on monitoring and correcting fluid and electrolyte levels.
📡Pharmacodynamics — effects in the body▾
When swallowed, the unabsorbed PEG, ascorbate, and sulfate ions create a strong osmotic effect in the colon — pulling water into the bowel and keeping it there. This produces a large volume of watery diarrhea that flushes the colon clean. The first bowel movement typically occurs about 1 to 2 hours after starting PLENVU, and the effect is rapid and thorough by design.
🔬Pharmacokinetics — how your body processes it▾
Most of the PEG-3350 in these preparations stays in the gut and is excreted in the stool — studies show 85% to 99% of the PEG dose leaves the body in the feces. Similarly, the majority of ascorbate (about 69%) and sodium sulfate (69–73%) are eliminated in stool, with some ascorbate and sulfate also appearing in urine. PEG-3350 that is absorbed has a half-life (the time for the body to clear half of it) of about 4 hours; ascorbate has a half-life of about 7 hours; and sulfate about 10.5 hours. Because so little is absorbed into the bloodstream, these preparations act mainly within the digestive tract rather than throughout the body.
📦How to store it▾
Store pack at room temperature, between 68°F to 77°F (20°C to 25°C) with excursions permitted to 59°F to 86°F (15°C to 30°C) . stored in a refrigerator.
📄 Written from Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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 Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / Sodium Sulfate — the kind of thing our pharmacy team would talk through with you at the counter.
What exactly is this prep for — is it a laxative I'll take regularly? ▾
When will I actually start going to the bathroom after I take it? ▾
Do I need to fast completely, or can I eat something? ▾
What should I do with my regular daily medications while taking this prep? ▾
What side effects should I just expect versus ones that mean I need to call someone? ▾
I'm pregnant — is this prep safe to take? ▾
Is Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / Sodium Sulfate available over the counter? ▾
When was Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / Sodium Sulfate first available? ▾
Who makes Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / Sodium Sulfate? ▾
💬 Answers drafted from Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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
📊 Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / Sodium Sulfate across the U.S. market
How Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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.
Also listed with the FDA, not a patient dose form: Kit (9) — bulk drug substance sold to compounders/manufacturers and multi-item kits. These aren’t counted in the dose-form total above.
Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
📈 How widely Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / Sodium Sulfate is used
A general measure of how commonly Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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 Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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 Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / Sodium Sulfate prescribed? Of the 1,596 medications we measure, Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / Sodium Sulfate ranks #930 by Medicaid prescriptions — more than 42% of them.
Utilization by Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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.
ascorbic acid 4700 MG / polyethylene glycol 3350 100000 MG / potassium chloride 1015 MG / sodium ascorbate 5900 MG / sodium chloride 2690 MG / sodium sulfate 7500 MG Powder for Oral Solution
Summed across the 3 of 5 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 800915
Other Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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 1 of 2 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 Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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 4 of 7 listed Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / Sodium Sulfate NDCs with Medicaid activity.
🔍 Compare Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / Sodium Sulfate products
A representative set of FDA-listed product records for Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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.)
| Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|
| 💊Kits | ||
| Oceanside Pharmaceuticals × 2 listings | NDA | View NDC → |
| Oceanside Pharmaceuticals | NDA AUTHORIZED GENERIC | View NDC → |
| Salix Pharmaceuticals, Inc × 3 listings | NDA | View NDC → |
| Salix Pharmaceuticals, Inc. × 3 listings | NDA | View NDC → |
Showing 9 of 9 products — FDA National Drug Code Directory. See every product, package size and price: browse all 9 Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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 Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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 Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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 Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one exact multiple-ingredient concept (MIN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). A product with a different ingredient combination belongs on a different page.
RxCUI 1007544 1 dose form · 1 strength
-
Dose form (SCDF) Powder for Oral Solution RxCUI 1870185No current FDA listingClinical drug / strength (SCD) ascorbic acid 4700 MG / polyethylene glycol 3350 100000 MG / potassium chloride 1015 MG / sodium ascorbate 5900 MG / sodium chloride 2690 MG / sodium sulfate 7500 MGRxCUI 800915
Look up RxCUI 1007544 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
📦 Supply & shortage status
Whether Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / 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
RxNorm drug class
Ascorbic Acid / Polyethylene Glycol 3350 / Potassium Chloride / Sodium Ascorbate / Sodium Chloride / Sodium Sulfate belongs to the Vitamin C class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
🔬 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 3 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. Salix Pharmaceuticals, 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.