GAVILYTE G

Manufacturer
Lupin Pharmaceuticals,Inc. | Novel Laboratories, Inc.
Effective date
2025-09-10
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-05-31 21:42:40

Label at a glance#

ProductGAVILYTE G TM
Active ingredientPOLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, SODIUM CHLORIDE, POTASSIUM CHLORIDE
Label structure14 sections

Indications and uses

GaviLyte-G is indicated for bowel cleansing prior to colonoscopy and barium enema X-ray examination in adults.

Dosage and administration

Correct fluid and electrolyte abnormalities before treatment with Gavilyte-G [ see Warnings and Precautions ( 5.1 )]. Reconstitute Gavilyte-G with water prior to ingestion, do not take undissolved Gavilyte-G [ see Dosage and Administration ( 2.2 )]. Do not reconstitute with other liquids and/or add starch-based thickeners to the mixing container [ see Warnings and Precautions ( 5.7 )]. Do not take oral medications...

Storage and handling

Gavilyte-G (polyethylene glycol 3350 and electrolytes for oral solution) is supplied in a 4-liter disposable jug containing 236 g polyethylene glycol 3350, 22.74 g sodium sulfate (anhydrous), 6.74 g sodium bicarbonate, 5.86 g sodium chloride and 2.97 g potassium chloride as a white to off white powder.   When reconstituted with water to a volume of 4 liters, the solution contains 59 g/L PEG3350, 5.69 g/L sodium su...

Label contents#

Full prescribing information#

1 INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

SPL UNCLASSIFIED SECTION

GaviLyte-G is indicated for bowel cleansing prior to colonoscopy and barium enema X-ray examination in adults.

2 DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

2.1 Important Preparation and Administration Instructions

  • Correct fluid and electrolyte abnormalities before treatment with Gavilyte-G [see Warnings and Precautions (5.1)].
  • Reconstitute Gavilyte-G with water prior to ingestion, do not take undissolved Gavilyte-G [see Dosage and Administration (2.2)]. Do not reconstitute with other liquids and/or add starch-based thickeners to the mixing container [see Warnings and Precautions (5.7)].
  • Do not take oral medications within 1 hour before the start of or during administration of Gavilyte-G [see Drug Interactions (7.2)].
  • Do not take other laxatives while taking Gavilyte-G [see Drug Interactions (7.3)]. Consume only clear liquids, avoid red and purple liquids.
  • Patients may consume water or other clear liquids during the bowel preparation and after completion of the bowel preparation up until 2 hours before the time of the colonoscopy.
  • The solution is more palatable if chilled prior to administration.
  • Do not consume solid food within 2 hours before starting Gavilyte-G. For the best results, do not consume solid food for 3 to 4 hours before drinking the solution.
  • If severe bloating, distention or abdominal pain occurs, slow or temporarily discontinue Gavilyte-G until the symptoms abate.

2.2 Dosage Regimen

Instruct adult patients that on the day before the colonoscopy procedure, they may consume a light breakfast at least 2 hours before starting Gavilyte-G. Begin the recommended dosage regiment for Gavilyte-G early in the evening on the day before colonoscopy.

Instruct patients to take Gavilyte-G in conjunction with clear liquids as follows:

This preparation can be used with or without the lemon flavor pack.

The pharmacist will add the lemon flavor pack prior to dispensing

(see packet instructions)

4 Liter Jug

  • Fill the supplied container containing the Gavilyte-G powder with lukewarm drinking water to the 4-liter fill line
  • Do not add any other ingredients, flavors, etc.
  • After capping the container, shake vigorously several times to ensure that the ingredients are dissolved.
  • Drink at a rate of 8 ounces every 10 minutes until the entire contents are consumed or the rectal effluent is clear. A loose watery bowel movement should result in approximately one hour.
  • After reconstitution, keep solution refrigerated 2° to 8°C (36° to 46°F). Do not freeze. Use within 48 hours, discard unused portion.

Administration via a Nasogastric Tube For patients with a nasogastric tube, administer the reconstituted Gavilyte-G solution at a rate of 20 to 30 mL per minute (1.2 to 1.8 liters per hour).

3 DOSAGE FORMS AND STRENGTHS

DOSAGE FORMS & STRENGTHS SECTION

SPL UNCLASSIFIED SECTION

For Oral Solution: 236 g polyethylene glycol 3350, 22.74 g sodium sulfate (anhydrous), 6.74 g sodium bicarbonate, 5.86 g sodium chloride and 2.97 g potassium chloride as a white to off-white powder. When reconstituted with water to a volume of 4 liters, the solution contains 59 g/L PEG-3350, 5.69 g/L sodium sulfate, 1.69 g/L sodium bicarbonate, 1.47 g/L sodium chloride and 0.743 g/L potassium chloride.

4 CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

SPL UNCLASSIFIED SECTION

GaviLyte-G is contraindicated in the following conditions:

  • Gastrointestinal (GI) obstruction [see Warnings and Precautions (5.6)]
  • Bowel perforation [see Warnings and Precautions (5.6)]
  • Toxic colitis or toxic megacolon
  • Gastric retention
  • Ileus
  • Hypersensitivity to any component of Gavilyte-G [see Warnings and Precautions (5.8)]

5 WARNINGS AND PRECAUTIONS

WARNINGS AND PRECAUTIONS SECTION

5.1 Serious Fluid and Serum Chemistry Abnormalities

Advise patients to hydrate adequately before, during, and after the use of GaviLyte-G. Use caution in patients with congestive heart failure when replacing fluids. If a patient develops significant vomiting or signs of dehydration including signs of orthostatic hypotension after taking GaviLyte-G, consider performing post-colonoscopy lab tests (electrolytes, creatinine, and BUN) and treat accordingly. Fluid and electrolyte disturbances can lead to serious adverse events including cardiac arrhythmias, seizures and renal impairment.Correct Fluid and electrolyte abnormalities before treatment with GaviLyte-G.

In addition, use caution when prescribing GaviLyte-G for patients who have conditions, or who are using medications, that increase the risk for fluid and electrolyte disturbances or may increase the risk of adverse events of seizure, arrhythmias, and renal impairment [see Drug Interactions (7.1) ]

5.2 Cardiac Arrhythmias

There have been rare reports of serious arrhythmias associated with the use of ionic osmotic laxative products for bowel preparation. Use caution when prescribing GaviLyte-G for patients at increased risk of arrhythmias (e.g., patients with a history of prolonged QT, uncontrolled arrhythmias, recent myocardial infarction, unstable angina, congestive heart failure, or cardiomyopathy). Consider pre-dose and post-colonoscopy ECGs in patients at increased risk of serious cardiac arrhythmias.

5.3 Seizures

There have been reports of generalized tonic-clonic seizures and/or loss of consciousness associated with use of bowel preparation products in patients with no prior history of seizures. The seizure cases were associated with electrolyte abnormalities (e.g., hyponatremia, hypokalemia, hypocalcemia, and hypomagnesemia) and low serum osmolality. The neurologic abnormalities resolved with correction of fluid and electrolyte abnormalities.

Use caution when prescribing GaviLyte-G for patients with a history of seizures and in patients at increased risk of seizure, such as patients taking medications that lower the seizure threshold (e.g., tricyclic antidepressants), patients withdrawing from alcohol or benzodiazepines, or patients with known or suspected hyponatremia. [see Drug Interactions (7.1)]

5.4 Renal Impairment

Use caution when prescribing GaviLyte-G for patients with impaired renal function or patients taking concomitant medications that may affect renal function (such as diuretics, angiotensin converting enzyme inhibitors, angiotensin receptor blockers, or non-steroidal anti-inflammatory drugs) [see Drug Intersections (7.1)]. Advise these patients of the importance of adequate hydration, and consider performing baseline and post-colonoscopy laboratory tests (electrolytes, creatinine, and BUN) in these patients. [see Use is Specific Populations (8.6)].

5.5 Colonic Mucosal Ulcerations and Ischemic Colitis

Administration of osmotic laxative products may produce colonic mucosal aphthous ulcerations, and there have been reports of more serious cases of ischemic colitis requiring hospitalization. Concurrent use of stimulant laxatives and GaviLyte-G may increase this risk[see Drug Interactions (7.3)]. Consider the potential for mucosal ulcerations resulting from the bowel preparation when interpreting colonoscopy findings in patients with known or suspect inflammatory bowel disease (IBD).

5.6 Use in Patients with Significant Gastrointestinal Disease

If gastrointestinal obstruction or perforation is suspected, perform appropriate diagnostic studies to rule out these conditions before administering GaviLyte-G. [see Contraindications (4)].

Use with caution in patients with severe active ulcerative colitis.

5.7 Aspiration

Use with caution in patients with impaired gag reflex, unconscious, or semiconscious patients, and patients prone to regurgitation or aspiration. Observe these patients during administration of  GaviLyte-G,  especially if it is administered via nasogastric tube.

Do not combine GaviLyte-G with starch-based thickeners [see Dosage and Administration (2.1)]. Polyethylene glycol (PEG), a component of GaviLyte-G, when mixed with starch-thickened liquids reduces the viscosity of the starch-thickened liquid. When a PEG-based product used for another indication was mixed in starch-based pre-thickened liquids used in patients with dysphagia, thinning of the liquid occurred and cases of chocking and potential aspiration were reported.

5.8 Hypersensitivity Reactions

Gavilyte-G contains PEG and may cause serious hypersensitivity reactions including anaphylaxis, angioedema, rash, urticaria, and pruritus [see Adverse Reactions (6 )]. Inform patients of the signs and symptoms of anaphylaxis and instruct them to seek immediate medical care should signs and symptoms occur.

6 ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

SPL UNCLASSIFIED SECTION

The following clinically significant adverse reactions are described elsewhere in the labeling:

  • Renal impairment [see Warnings and Precautions (5.4)]
  • Colonic mucosal ulcerations and ischemic colitis [see Warnings
  • and Precautions (5.5)]
  • Patients with significant gastrointestinal disease [see Warnings
  • and Precautions (5.6)]
  • Aspiration [see Warnings and Precautions (5.7)]

The following adverse reactions associated with the use of Gavilyte-G were identified in clinical trials or postmarketing reports. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to estimate their frequency, reliably, or establish a causal relationship to drug exposure.

  •   Cardiovascular: arrhythmia, atrial fibrillation, peripheral edema, asystole, and acute pulmonary edema after aspiration [see Warnings and Precautions (5.2)].
  •   Nervous system: tremor, seizure [see Warnings and Precautions (5.3)]
  •   Hypersensitivity: Urticaria/rash, pruritus, dermatitis, rhinorrhea, dyspnea, chest and throat tightness, fever, angioedema, anaphylaxis and anaphylactic shock [see Contraindications (4), Warnings and Precautions (5.8)]
  •   Gastrointestinal: Nausea, abdominal fullness and bloating are the most common adverse reactions (occurred in up to 50% of patients). Other less common adverse reactions include: abdominal cramps, vomiting, "butterfly-like" infiltrates on chest X-ray after vomiting and aspirating PEG, anal irritation, and upper GI bleeding from Mallory-Weiss Tear, esophageal perforation [usually with gastroesophageal reflux disease (GERD)].

7 DRUG INTERACTIONS

DRUG INTERACTIONS SECTION

7.1 Drugs that May Increase Risks Due to Fluid and Electrolyte Abnormalities

Use caution when prescribing GaviLyte-G for patients with conditions and/or who are using medications that increase the risk for fluid and electrolyte disturbances or may increase the risk of renal impairment, seizure, arrhythmias, and prolonged QT in the setting of fluid and electrolyte abnormalities. [see Warnings and Precautions (5.1, 5.2, 5.3, 5.4)]. Consider additional patient evaluations as appropriate.

7.2 Potential for Reduced Drug Absorption

Gavilyte-G can reduce the absorption of other administered drugs. Administer oral medications within one hour before the start of administration of Gavilyte-G [see Dosage and Administration (2.1)].

7.3 Stimulant Laxatives

Concurrent use of stimulant laxatives and GaviLyte-G may increase the risk of mucosal ulceration or ischemic colitis. Avoid use of stimulant laxatives (e.g., bisacodyl, sodium picosulfate) while taking Gavilyte-G [see Warnings and Precautions (5.5)].

8 USE IN SPECIFIC POPULATIONS

USE IN SPECIFIC POPULATIONS SECTION

8.1 Pregnancy

PREGNANCY SECTION

Animal reproduction studies have not been conducted with GaviLyte-G. It is also not known whether GaviLyte-G can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity. GaviLyte-G should be given to a pregnant woman only if clearly needed.

8.3 Nursing Mothers

NURSING MOTHERS SECTION

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 GaviLyte-G is administered to a nursing woman.

8.4 Pediatric Use

PEDIATRIC USE SECTION

Safety and effectiveness of GaviLyte-G in pediatric patients have not been established.

8.5 Geriatric Use

GERIATRIC USE SECTION

Clinical studies of GaviLyte-G did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients.

8.6 Renal Impairment

Use Gavilyte-G with caution in patients with renal impairment or patients taking concomitant medications that may affect renal function [see Drug Interactions (7.1)]. These patients may be at risk for renal injury. Advise these patients of the importance of adequate hydration before, during and after use of Gavilyte-G and consider performing baseline and post-colonoscopy laboratory tests (electrolytes, creatinine, and BUN) in these patients [see Warnings and Precautions (5.4)].

11 DESCRIPTION

DESCRIPTION SECTION

Gavilyte-G is a combination of polyethylene glycol 3350, an osmotic laxative, and electrolytes (sodium sulfate, sodium chloride, sodium bicarbonate and potassium chloride) for oral solution supplied in a 4 liter disposable jug containing 236 g polyethylene glycol 3350, 22.74 g sodium sulfate (anhydrous), 6.74 g sodium bicarbonate, 5.86 g sodium chloride, and 2.97 g potassium chloride as a white to off-white powder.

Polyethylene Glycol 3350, NF

a
a

Sodium Sulfate, USP

The chemical name is Na2SO4. The average Molecular Weight is 142.04. The structural formula is:

b
b

Sodium Bicarbonate, USP

The chemical name is NaHCO3. The average Molecular Weight is 84.01. The structural formula is:

c
c

Sodium Chloride, USP

The chemical name is NaCl. The average Molecular Weight: 58.44. The structural formula is:

Na+ Cl-

Potassium Chloride, USP

The chemical name is KCl. The average Molecular Weight: 74.55. The structural formula is:

K-Cl

12 CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

12.1 Mechanism of Action

MECHANISM OF ACTION SECTION

The primary mode of action is thought to be through the osmotic effect of polyethylene glycol 3350 which causes water to be retained in the colon and produces a watery stool.

12.2 Pharmacodynamics

PHARMACODYNAMICS SECTION

GaviLyte-G induces as diarrhea which rapidly cleanses the bowel, usually within four hours.

12.3 Pharmacokinetics

PHARMACOKINETICS SECTION

The pharmacokinetics of PEG 3350 following administration of GaviLyte-G were not assessed. Available pharmacokinetic information for oral PEG 3350 suggests that it is poorly absorbed.

16 HOW SUPPLIED/STORAGE AND HANDLING

HOW SUPPLIED SECTION

Gavilyte-G (polyethylene glycol 3350 and electrolytes for oral solution) is supplied in a 4-liter disposable jug containing 236 g polyethylene glycol 3350, 22.74 g sodium sulfate (anhydrous), 6.74 g sodium bicarbonate, 5.86 g sodium chloride and 2.97 g potassium chloride as a white to off white powder.

  •   When reconstituted with water to a volume of 4 liters, the solution contains 59 g/L PEG3350, 5.69 g/L sodium sulfate, 1.69 g/L sodium bicarbonate, 1.47 g/L sodium chloride and 0.743 g/L potassium chloride.

Gavilyte-G 4 Liter Disposable Jug                                                                                 NDC 43386-090-19

Storage

Store in sealed container at 15° to 30°C (59° to 86°F). Store reconstituted solution of Gavilyte-G at 2° to 8°C (36° to 46°F). Do not freeze [see Dosage and Administration (2.1)].

17 PATIENT COUNSELING INFORMATION

INFORMATION FOR PATIENTS SECTION

Advise the patient to read the FDA-Approved Patient Labeling (Medication Guide and Instructions for Use).

Instruct patients:

  • To reconstitute Gavilyte-G with water prior to ingestion.
  • Not to take other laxatives while they are taking Gavilyte-G.
  • Not to take oral medications within 1 hour before the start or during the administration of Gavilyte-G.
  • To take only clear liquids but avoid red and purple liquids.
  • To consume water or other clear liquids during the bowel preparation and after completion of the bowel preparation up until 2 hours before the time of the colonoscopy.
  • To follow the directions in the Instructions for Use on how to prepare and administer the product.
  • If they experience severe bloating, distention or abdominal pain, to slow or temporarily discontinue drinking the solution and to contact their healthcare provider.
  • To contact their healthcare provider if they develop signs and symptoms of dehydration or if they experience altered consciousness or seizures. [see Warnings and Precautions (5.1, 5.2, 5.3, 5.4)].
  • To discontinue administration of the solution and contact their healthcare provider if they develop symptoms of a hypersensitivity reaction [see Warnings and Precautions (5.8)].

LUPIN and the 17 PATIENT COUNSELING INFORMATION17 PATIENT COUNSELING INFORMATION are registered trademarks of Lupin Pharmaceuticals, Inc.

Manufactured by:

Novel Laboratories, Inc.

Somerset, NJ 08873

Manufactured for:

Lupin Pharmaceuticals, Inc.

Naples FL, 34108

SAP code: 278923

Rev: 11/2024

MEDICATION GUIDE

SPL MEDGUIDE SECTION

SPL UNCLASSIFIED SECTION

GaviLyte™-G (GAV-ee-LITE-G)

(PEG-3350 (236 g) and Electrolytes for Oral Solution, USP)

Read this Medication Guide before you start taking GaviLyte-G. This information does not take the place of talking with your healthcare provider about your medical condition or your treatment.

SPL UNCLASSIFIED SECTION

What is the most important information I should know about GaviLyte-G?

GaviLyte-G and other osmotic bowel preparations can cause serious side effects, including:

Serious loss of body fluid (dehydration) and changes in blood salts (electrolytes) in your blood.

These changes can cause:

  • abnormal heartbeats (arrhythmias)  that can cause death
  • seizures. This can happen even if you have never had a seizure.
  • kidney problems

Your chance of having fluid loss and changes in body salts with GaviLyte-G is higher if you:

  • have heart problems
  • have kidney problems
  • take water pills or non-steroidal anti-inflammatory drugs (NSAIDS)

Tell your healthcare provider right away if you have any of these symptoms of a loss of too much body fluid (dehydration) while taking GaviLyte-G:

  • vomiting that prevents you from keeping down the solution
  • dizziness
  • urinating less often than normal
  • headache

See Section "what are the possible side effects of GaviLyte-G?" for more information about side effects.

SPL UNCLASSIFIED SECTION

What is GaviLyte-G?

GaviLyte-G is a prescription medicine used by adults to clean the colon before a colonoscopy or barium enema X-ray examination. GaviLyte-G cleans your colon by causing you to have diarrhea (loose stools). Cleaning your colon helps your healthcare provider see the inside of your colon more clearly during your colonoscopy.

It is not known if GaviLyte-G is safe and effective in children.

Who should not take GaviLyte-G?

Do not take GaviLyte-G if your heathcare provider has told you that you have:

  • a blockage in your bowel (obstruction)
  • an opening in the wall of your stomach or intestine (bowel perforation)
  • problems with food and fluid emptying from your stomach (gastric retention)
  • a very dilated intestine (toxic megacolon)
  • problems with food and fluid emptying from your stomach (gastric retention).
  • a problem with food moving too slowly through your intestines (ileus).
  • an allergy to any of the ingredients in GaviLyte-G. See the end of this Medication Guide for a complete list of ingredients in GaviLyte-G.

What should I tell my healthcare provider before taking GaviLyte-G?

Before you take GaviLyte-G, tell your healthcare provider if you:

  • have heart problems
  • have stomach or bowel problems
  • have ulcerative colitis
  • have problems with swallowing or gastric reflux
  • have a history of seizures
  • are withdrawing from drinking alcohol
  • have a low blood salt (sodium) level
  • have kidney problems
  • have any other medical conditions
  • are pregnant. It is not known if GaviLyte-G will harm your unborn baby. Talk to your doctor if you are pregnant or plan to become pregnant.
  • are breastfeeding or plan to breastfeed. It is not known if GaviLyte-G passes into your breast milk. You and your healthcare provider should decide if you will take GaviLyte-G while breastfeeding.

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.

GaviLyte-G may affect how other medicines work. Do not take medicines by mouth within 1 hour of starting Gavilyte-G or after you start taking

Gavilyte-G.

Especially tell your healthcare provider if you take:

  • medicines for blood pressure or heart problems
  • medicines for kidney problems
  • medicines for seizures
  • water pills (diuretics)
  • non-steroidal anti-inflammatory medicines (NSAID) pain medicines
  • laxatives
  • starch-based thickeners. For patients who have trouble swallowing, do not mix Gavilyte-G with starch-based thickeners.

Ask your healthcare provider or pharmacist for a list of these medicines if you are not sure if you are taking any of the medicines listed above.

Know the medicines you take. Keep a list of them to show your healthcare provider and pharmacist when you get a new medicine.

SPL UNCLASSIFIED SECTION

How should I take GaviLyte-G?

You must read, understand, and follow these instructions to take GaviLyte-G the right way.

  • Take GaviLyte-G exactly as your healthcare provider tells you to take it.
  • See the "Instructions for Use" on the bottle label for instructions on how to mix, take or give Gavilyte-G.
  • Do not take undissolved GaviLyte-G powder that has not been mixed with water (diluted), it may increase your risk of nausea, vomiting and fluid loss (dehydration).
  • Do not take other laxatives while taking Gavilyte-G.
  • Drink reconstituted solution at a rate of 8 ounces (240 ml) every 10 minutes. Rapid drinking of each portion is better than drinking small amounts.
  • Do not eat or drink anything colored red or purple.
  • Do not eat solid foods at least 2 hours before taking Gavilyte-G. You may eat a light breakfast 2 hours before taking Gavilyte-G. For best results, do not consume solid food for 3 to 4 hours before drinking Gavilyte-G.
  • Drink only water and clear liquids:
  • the day before your colonoscopy
  • while taking Gavilyte-G
  • after taking Gavilyte-G until 2 hours before your colonoscopy.
  • Drink clear liquids before, during, and after you take Gavilyte-G to avoid fluid loss (dehydrated). Examples of clear liquids are:
  • water
  • clear broth
  • clear fruit juices without pulp including apple, white grape, or white cranberry
  • clear soda
  • strained limeade or lemonade
  • gelatin (without added fruit or topping)
  • coffee or tea (Do not use any dairy or non-dairy creamer)
  • popsicles without pieces of fruit or fruit pulp
  • You may experience some abdominal bloating and distention before the bowels start to move. If severe discomfort or distention occur, slow or temporarily stop (discontinue) drinking the solution and contact your healthcare provider.
  • The first bowel movement should occur approximately one hour after you start drinking the solution.
  • Continue drinking until the watery stool is clear and free of solid matter.

SPL UNCLASSIFIED SECTION

What are the possible side effects of GaviLyte-G?

GaviLyte-G can cause serious side effects, including:

  • See Section "what is the most important information I should know about GaviLyte-G?"
  • changes in certain blood tests. Your healthcare provider may do blood tests before and after you take GaviLyte-G to check your blood for changes. Tell your healthcare provider if you have any symptoms of too much fluid loss, including:
  • vomiting
  • nausea
  • bloating
  • dizziness
  • stomach (abdominal) cramping
  • headache
  • urinate less than usual
  • trouble drinking clear liquid
  • ulcers of the bowel or bowel problems (ischemic colitis). Tell your healthcare provider right away if you have severe stomach-area (abdomen) pain or rectal bleeding.

The most common side effects of GaviLyte-G include:

  • nausea
  • stomach (abdominal) fullness
  • bloating
  • stomach (abdominal) cramps
  • vomiting
  • chest x-ray that shows water in the lungs (infiltrate) after vomiting or inhaling food or liquid (aspirate).  
  • anal irritation
  • esophageal bleeding

Tell your healthcare provider if you have any side effect that bothers you or that does not go away.

These are not all the possible side effects of GaviLyte-G. For more information, ask your healthcare provider or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

SPL UNCLASSIFIED SECTION

How should I store GaviLyte-G?

  • Store Gavilyte-G in a sealed container at room temperature, between 59°F to 86°F (15°C to 30°C).
  • Store mixed (reconstituted) solution of Gavilyte-G at 36° to 46°F (2°C to 8°C). Do not freeze.
  • Use mixed (reconstituted) solution of Gavilyte-G within 48 hours.
  • After 48 hours, throw away (discard) any mixed (reconstituted) solution of Gavilyte-G that is not used.

Keep GaviLyte-G and all medicines out of the reach of children.

General information about the safe and effective use of GaviLyte-G.

Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use GaviLyte-G for a condition for which it was not prescribed. Do not give GaviLyte-G to other people, even if they are going to have the same procedure you are. It may harm them.

This Medication Guide summarizes important information about GaviLyte-G. If you would like more information, talk with your healthcare provider. You can ask your pharmacist or healthcare provider for information that is written for healthcare professionals.

SPL UNCLASSIFIED SECTION

What are the ingredients in GaviLyte-G?

Gavilyte-G comes in a 4-liter jug with Gavilyte-G powder.

Active ingredients: polyethylene glycol 3350, sodium sulfate, sodium bicarbonate, sodium chloride, and potassium chloride.

Inactive ingredients: Lemon Flavored GaviLyte-G only (natural lemon flavor, maltodextrin, sodium saccharin)

This Medication Guide has been approved by the U.S. Food and Drug Administration.

For more information call 1-866-403-7592.

LUPIN and the SPL UNCLASSIFIED SECTIONSPL UNCLASSIFIED SECTION are registered trademarks of Lupin Pharmaceuticals, Inc.

Manufactured by:

Novel Laboratories, Inc.

Somerset, NJ 08873

Manufactured for:

Lupin Pharmaceuticals, Inc.

Naples FL, 34108

SAP code: 278923

Rev: 11/2024

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GaviLyte-G

Container Label

label
label

Lemon Flavor Pack

Lemon Flavor Pack
Lemon Flavor Pack

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
967012Gavilyte-G Powder for Oral SolutionPSN9
966920polyethylene glycol 3350 236 GM / potassium chloride 2.97 GM / sodium bicarbonate 6.74 GM / sodium chloride 5.86 GM / sodium sulfate 22.74 GM Powder for Oral SolutionPSN9
967012polyethylene glycol 3350 236000 MG / potassium chloride 2970 MG / sodium bicarbonate 6740 MG / sodium chloride 5860 MG / sodium sulfate 22740 MG Powder for Oral Solution [Gavilyte-G]SBD9
966920polyethylene glycol 3350 236000 MG / potassium chloride 2970 MG / sodium bicarbonate 6740 MG / sodium chloride 5860 MG / sodium sulfate 22740 MG Powder for Oral SolutionSCD9
967012Gavilyte-G (polyethylene glycol 3350 236 GM / potassium chloride 2.97 GM / sodium bicarbonate 6.74 GM / sodium chloride 5.86 GM / sodium sulfate 22.74 GM) Powder for Oral SolutionSY9
966920polyethylene glycol 3350 236 GM / potassium chloride 2.97 GM / sodium bicarbonate 6.74 GM / sodium chloride 5.86 GM / sodium sulfate 22.74 GM Powder for Oral SolutionSY9
966920POLYETHYLENE GLYCOL 3350 236000 MG / K+ Chloride 2970 MG / NaHCO3 6740 MG / NaCl 5860 MG / sodium sulfate 22740 MG Powder for Oral SolutionSY9
967012POLYETHYLENE GLYCOL 3350 236000 MG / K+ Chloride 2970 MG / NaHCO3 6740 MG / NaCl 5860 MG / sodium sulfate 22740 MG Powder for Oral Solution [Gavilyte-G]SY9
966920POLYETHYLENE GLYCOL 3350 236000 MG / Pot Chloride 2970 MG / NaHCO3 6740 MG / NaCl 5860 MG / sodium sulfate 22740 MG Powder for Oral SolutionSY9
967012POLYETHYLENE GLYCOL 3350 236000 MG / Pot Chloride 2970 MG / NaHCO3 6740 MG / NaCl 5860 MG / sodium sulfate 22740 MG Powder for Oral Solution [Gavilyte-G]SY9

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
POLYETHYLENE GLYCOL 3350 Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
POTASSIUM CATION Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813
SODIUM CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9e37788c-b1bf-42ae-aac9-b60601606144Product name820260122
95250459-30e4-45c1-b08a-993044f49109Product name220250805
d9771140-739b-484b-ae64-b79528ff1211Product name320250801
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
1527ac37-808d-43be-a63e-74e1258dbe46Product name920250219
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
bed0530e-f939-4541-956b-6928a2f6404fProduct name120241008
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name620240814
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
9fcb7a91-de07-4f00-aabf-e4d6fda403d5Product name820230322
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
7916de40-e296-41f0-b811-6d0df1a33e2cProduct name920180627
cefa60e2-a5b5-493e-9c54-24735b7dc509Product name220171212
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
d723478e-ad4a-ec23-6bd7-cfe33e1e3840Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43386-090-19GAVILYTE GTM274.31 g in 1 BOTTLEPOWDER, FOR SOLUTION274.319

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
43386-090-19ML - Milliliter43386-0905e525291-10ca-410e-bed1-3abd130a8a8d12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
POLYETHYLENE GLYCOL 3350ACTIVE INGREDIENTG2M7P15E5P1
POTASSIUM CHLORIDEACTIVE INGREDIENT660YQ98I101
SODIUM BICARBONATEACTIVE INGREDIENT8MDF5V39QO1
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X1
SODIUM SULFATE ANHYDROUSACTIVE INGREDIENT36KCS0R7501
CHLORIDE IONACTIVE MOIETYQ32ZN486981
POLYETHYLENE GLYCOL 3350ACTIVE MOIETYG2M7P15E5P1
POTASSIUM CATIONACTIVE MOIETY295O53K1521
SODIUM CATIONACTIVE MOIETYLYR4M0NH371
SULFATE IONACTIVE MOIETY7IS9N8KPMG1
ACACIAINACTIVE INGREDIENT5C5403N26O1
ALPHA-TOCOPHEROL, DL-INACTIVE INGREDIENT7QWA1RIO011
MALTODEXTRININACTIVE INGREDIENT7CVR7L4A2D1
SACCHARIN SODIUMINACTIVE INGREDIENTSB8ZUX40TY1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43386-09043386-090-19

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 46 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALPHA-TOCOPHEROL, DL-.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01SUSPENSION / ORAL0.01 mg/1mlExact identifier — unii+route
12 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET, FILM COATED, EXTENDED RELEASE / ORALNAExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DGRANULE, FOR SUSPENSION / ORAL952 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DPOWDER, FOR SUSPENSION / ORAL8000 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DPASTE / ORAL1050 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DSUSPENSION / ORAL6040 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET / ORAL320 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET, EXTENDED RELEASE / ORAL3239 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET, COATED / ORAL5.6 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DLOZENGE / ORAL175 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DGRANULE, FOR SUSPENSION / ORAL952 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DCAPSULE / ORAL200 mgExact identifier — unii+route
30 equally ranked IID candidates
SACCHARIN SODIUMSACCHARIN SODIUMSB8ZUX40TYPOWDER, FOR SOLUTION / ORAL199 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALPHA-TOCOPHEROL, DL-.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01SUSPENSION / ORAL0.01 mg/1mlExact identifier — unii+route
12 equally ranked IID candidates
SACCHARIN SODIUMSACCHARIN SODIUMSB8ZUX40TYPOWDER, FOR SOLUTION / ORAL199 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALPHA-TOCOPHEROL, DL-.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01CAPSULE / ORAL90 mgExact identifier — unii+route
12 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET, FILM COATED, EXTENDED RELEASE / ORALNAExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET, ORALLY DISINTEGRATING / ORAL12 mgExact identifier — unii+route
30 equally ranked IID candidates
ALPHA-TOCOPHEROL, DL-.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01TABLET / ORAL0.12 mgExact identifier — unii+route
12 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DFILM, SOLUBLE / ORAL19 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET, EFFERVESCENT / ORAL14404 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DSOLUTION / ORAL1451 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET, CHEWABLE / ORAL292 mgExact identifier — unii+route
30 equally ranked IID candidates
ALPHA-TOCOPHEROL, DL-.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01TABLET / ORAL0.12 mgExact identifier — unii+route
12 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET / ORAL320 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET, ORALLY DISINTEGRATING / ORAL12 mgExact identifier — unii+route
30 equally ranked IID candidates
ACACIAACACIA5C5403N26OPOWDER, FOR SOLUTION / ORALNAExact identifier — unii+route+dosage form
2 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DPOWDER, FOR SUSPENSION / ORAL8000 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DSUSPENSION / ORAL6040 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET, EFFERVESCENT / ORAL14404 mgExact identifier — unii+route
30 equally ranked IID candidates
ALPHA-TOCOPHEROL, DL-.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01TABLET, CHEWABLE / ORAL0.02 mgExact identifier — unii+route
12 equally ranked IID candidates
ALPHA-TOCOPHEROL, DL-.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01POWDER, FOR SUSPENSION / ORALNAExact identifier — unii+route
12 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DFILM, SOLUBLE / ORAL19 mgExact identifier — unii+route
30 equally ranked IID candidates
ALPHA-TOCOPHEROL, DL-.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01TABLET, CHEWABLE / ORAL0.02 mgExact identifier — unii+route
12 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DLOZENGE / ORAL175 mgExact identifier — unii+route
30 equally ranked IID candidates
ALPHA-TOCOPHEROL, DL-.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01SOLUTION / ORAL4 mgExact identifier — unii+route
12 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET, EXTENDED RELEASE / ORAL3239 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DSOLUTION / ORAL1451 mgExact identifier — unii+route
30 equally ranked IID candidates
ALPHA-TOCOPHEROL, DL-.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01SOLUTION / ORAL4 mgExact identifier — unii+route
12 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DPASTE / ORAL1050 mgExact identifier — unii+route
30 equally ranked IID candidates
ALPHA-TOCOPHEROL, DL-.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01CAPSULE / ORAL90 mgExact identifier — unii+route
12 equally ranked IID candidates
ALPHA-TOCOPHEROL, DL-.ALPHA.-TOCOPHEROL, DL-7QWA1RIO01POWDER, FOR SUSPENSION / ORALNAExact identifier — unii+route
12 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET, CHEWABLE / ORAL292 mgExact identifier — unii+route
30 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DTABLET, COATED / ORAL5.6 mgExact identifier — unii+route
30 equally ranked IID candidates
ACACIAACACIA5C5403N26OPOWDER, FOR SOLUTION / ORALNAExact identifier — unii+route+dosage form
2 equally ranked IID candidates
MALTODEXTRINMALTODEXTRIN7CVR7L4A2DCAPSULE / ORAL200 mgExact identifier — unii+route
30 equally ranked IID candidates

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A090231-001PEG 3350 AND ELECTROLYTESPOLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE ANHYDROUS236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 1 matching rows.

Application-product, TE code table
Application-productTE code
A090231-001AA

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-0184e616aacf4f…
2026-08-18 06:07:402026-07A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-0131067a03dcf5…
2025-08-23 18:47 UTC2025-08A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-016a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-0103ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-012680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-015bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-0179d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-011e350fbaab3a…
2024-05-31 18:47 UTC2024-05A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-018072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-015c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-015d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-014b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-0174a2ff9319b5…
2022-03-09 01:35 UTC2022-03A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-0187673890dc5c…
2021-03-12 10:30 UTC2021-03A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-015aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-018869cabd3fbd…
2020-11-12 02:37 UTC2020-11A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01c0c555d07b60…
2019-12-14 00:12 UTC2019-12A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-013f01610625f2…
2019-09-15 20:21 UTC2019-09A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01b00525d2431f…
2019-07-19 19:46 UTC2019-07A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-016a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-011c564ffb4f44…
2023-12-20 04:57 UTC2023-12A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-019b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-013f0d92c62455…
2023-05-13 08:27 UTC2023-05A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01053a50430f4f…
2023-01-26 05:58 UTC2023-01A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-013bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-013a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A090231-001PEG 3350 AND ELECTROLYTES236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOTFOR SOLUTION / ORALAA2009-06-01f41ea6bd6efb…

Observed Orange Book normalized TE history#

Normalized TE history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2026-09-14 22:38:342026-08A090231-001AA184e616aacf4f…
2026-08-18 06:07:402026-07A090231-001AA1caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A090231-001AA1011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A090231-001AA131067a03dcf5…
2025-08-23 18:47 UTC2025-08A090231-001AA16a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A090231-001AA1fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A090231-001AA1b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A090231-001AA103ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A090231-001AA12680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A090231-001AA15bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A090231-001AA1d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A090231-001AA1d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A090231-001AA179d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A090231-001AA1301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A090231-001AA11e350fbaab3a…
2024-05-31 18:47 UTC2024-05A090231-001AA18072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A090231-001AA15c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A090231-001AA15d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A090231-001AA14b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A090231-001AA174a2ff9319b5…
2022-03-09 01:35 UTC2022-03A090231-001AA1bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A090231-001AA1782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A090231-001AA187673890dc5c…
2021-03-12 10:30 UTC2021-03A090231-001AA15aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A090231-001AA18869cabd3fbd…
2020-11-12 02:37 UTC2020-11A090231-001AA1c0c555d07b60…
2019-12-14 00:12 UTC2019-12A090231-001AA13f01610625f2…
2019-09-15 20:21 UTC2019-09A090231-001AA1b00525d2431f…
2019-07-19 19:46 UTC2019-07A090231-001AA1ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A090231-001AA16a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A090231-001AA11c564ffb4f44…
2023-12-20 04:57 UTC2023-12A090231-001AA1ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A090231-001AA1a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A090231-001AA19b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A090231-001AA1a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A090231-001AA13f0d92c62455…
2023-05-13 08:27 UTC2023-05A090231-001AA1053a50430f4f…
2023-01-26 05:58 UTC2023-01A090231-001AA13bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A090231-001AA13a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A090231-001AA1f41ea6bd6efb…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GAVILYTE G TMPOLYETHYLENE GLYCOL-3350 AND ELECTROLYTESLupin Pharmaceuticals,Inc.3978822b-6473-4072-9f80-20ceb9bea3552025-09-10Warnings, Adverse reactionsExact identifier
ndc (package): 43386-090-19
ndc (product): 43386-090
ndc11 (package): 43386009019
spl id: 896fc5ca-9a67-47c1-a317-f8dd4a3654c8
spl set id: 3978822b-6473-4072-9f80-20ceb9bea355

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.