Polyethylene Glycol 3350 NF Polyethylene Glycol 3350 Powder for Oral Solution

Manufacturer
Nexgen Pharma, Inc.
Effective date
2011-08-10
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 20:12:47

Key Label Information#

Uses

INDICATIONS AND USAGE

For the treatment of occasional constipation. This product should be used for 2 weeks or less or as directed by a physician.

CONTRAINDICATIONS

Polyethylene Glycol 3350 NF is contraindicated in patients with known or suspected bowel obstruction and patients known to be allergic to polyethylene glycol.

Warnings

CONTRAINDICATIONS

Polyethylene Glycol 3350 NF is contraindicated in patients with known or suspected bowel obstruction and patients known to be allergic to polyethylene glycol.

WARNINGS

Patients with symptoms suggestive of bowel obstruction (nausea, vomiting, abdominal pain or distention) should be evaluated to rule out this condition before initiating Polyethylene Glycol 3350 NF therapy.

Directions And Dosage

DOSAGE AND ADMINISTRATION

The usual dose is 17 grams (about 1 heaping tablespoon) of powder per day (or as directed by physician) in 4 to 8 ounces of water, juice, soda, coffee, or tea. Each bottle of Polyethylene Glycol 3350 NF is supplied with a dosing cup marked to contain 17 grams of laxative powder when filled to the indicated line. Two to 4 days (48 to 96 hours) may be required to produce a bowel movement.

Other Label Information

PRINCIPAL DISPLAY PANEL

Label Images#

71508b14-3d59-408c-b43c-aff2f47b8b3d-01
71508b14-3d59-408c-b43c-aff2f47b8b3d-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
876193polyethylene glycol 3350 17 GM Powder for Oral SolutionPSN2
876193polyethylene glycol 3350 17000 MG Powder for Oral SolutionSCD2
876193polyethylene glycol 3350 17 GM Powder for Oral SolutionSY2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
POLYETHYLENE GLYCOL 3350 Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
d723478e-ad4a-ec23-6bd7-cfe33e1e3840Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0722-6920-012020-01-31C16284748780-19d75b9d0-fb1a-f424-e053-dadaa90a57cePolyethylene Glycol 3350 NF Polyethylene Glycol 3350 Powder for Oral Solution

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0722-6920-01Polyethylene Glycol 3350255 in 1 BOTTLE, PLASTICPOWDER, FOR SOLUTION2552

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0722-6920POLYETHYLENE GLYCOL 3350 POWDER, FOR SOLUTION [NEXGEN PHARMA, INC.]2Legacy NDC, 1 package rows20110829_a71759de-123d-4984-93e6-35661ad7d739.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
POLYETHYLENE GLYCOL 3350ACTIVE INGREDIENTG2M7P15E5P2
POLYETHYLENE GLYCOL 3350ACTIVE MOIETYG2M7P15E5P2

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0722-69200722-6920-01

Ingredients#

Name, UNII, Kind table
NameUNIIKind
POLYETHYLENE GLYCOL 3350G2M7P15E5PACTIB

Complete SPL Sections#

DESCRIPTION

DESCRIPTION SECTION

A white powder for reconstitution. Polyethylene Glycol 3350 NF (Polyethylene Glycol 3350 Powder For Oral Solution) is a synthetic polyglycol having an average molecular weight of 3350. The actual molecular weight is not less than 90.0 percent and not greater than 110.0 percent of the nominal value. The chemical formula is HO(C2H4O)nH in which n represents the average number of oxyethylene groups. Below 55°C it is a free flowing white powder freely soluble in water. Polyethylene Glycol 3350 NF is an osmotic agent for the treatment of constipation.

CLINICAL PHARMACOLOGY

CLINICAL PHARMACOLOGY SECTION

Pharmacology: Polyethylene Glycol 3350 NF is an osmotic agent which causes water to be retained with the stool. Essentially, complete recovery of Polyethylene Glycol 3350 NF was shown in normal subjects without constipation. Attempts at recovery of Polyethylene Glycol 3350 NF in constipated patients resulted in incomplete and highly variable recovery. In vitro study showed indirectly that Polyethylene Glycol 3350 NF was not fermented into hydrogen or methane by the colonic microflora in human feces. Polyethylene Glycol 3350 NF appears to have no effect on the active absorption or secretion of glucose or electrolytes. There is no evidence of tachyphylaxis. CLINICAL TRIALS In one study, patients with less than 3 bowel movements per week were randomized to Polyethylene Glycol 3350 NF, 17 grams, or placebo for 14 days. An increase in bowel movement frequency was observed for both treatment groups during the first week of treatment. Polyethylene Glycol 3350 NF was statistically superior to placebo during the second week of treatment. In another study, patients with 3 bowel movements or less per week and/or less than 300 grams of stool per week were randomized to 2 dose levels of Polyethylene Glycol 3350 NF or placebo for 10 days each. Success was defined by an increase in both bowel movement frequency and daily stool weight. For both parameters, superiority of the 17 gram dose of Polyethylene Glycol 3350 NF over placebo was demonstrated.

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

For the treatment of occasional constipation. This product should be used for 2 weeks or less or as directed by a physician.

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

Polyethylene Glycol 3350 NF is contraindicated in patients with known or suspected bowel obstruction and patients known to be allergic to polyethylene glycol.

WARNINGS

WARNINGS SECTION

Patients with symptoms suggestive of bowel obstruction (nausea, vomiting, abdominal pain or distention) should be evaluated to rule out this condition before initiating Polyethylene Glycol 3350 NF therapy.

PRECAUTIONS

PRECAUTIONS SECTION

ADVERSE REACTIONS

ADVERSE REACTIONS SECTION

Nausea, abdominal bloating, cramping and flatulence may occur. High doses may produce diarrhea and excessive stool frequency, particularly in elderly nursing home patients. Patients taking other medications containing polyethylene glycol have occasionally developed urticaria suggestive of an allergic reaction.

DRUG ABUSE AND DEPENDENCE

DRUG ABUSE AND DEPENDENCE SECTION

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

The usual dose is 17 grams (about 1 heaping tablespoon) of powder per day (or as directed by physician) in 4 to 8 ounces of water, juice, soda, coffee, or tea. Each bottle of Polyethylene Glycol 3350 NF is supplied with a dosing cup marked to contain 17 grams of laxative powder when filled to the indicated line. Two to 4 days (48 to 96 hours) may be required to produce a bowel movement.

HOW SUPPLIED

HOW SUPPLIED SECTION

In powdered form, for oral administration after dissolution in water, juice, soda, coffee, or tea. Polyethylene Glycol 3350 NF (Polyethylene Glycol 3350 Powder for Oral Solution) is available in two package sizes: a 500 cc container of 255 grams of laxative powder and a 950 cc container of 527 grams of laxative powder. NDC 0722-6920-01 Polyethylene Glycol 3350 NF 255g NDC 0722-6921-01 Polyethylene Glycol 3350 NF 527g The dosing cup supplied with each bottle is marked with a measuring line and may be used to measure a single Polyethylene Glycol 3350 NF dose of 17 grams (about 1 heaping tablespoonful). Rx only Keep this and all medications out of the reach of children. STORAGE Store at 20°- 25°C (68°- 77°F); excursions permitted to 15° - 30°C (59° - 86°F). [See USP Controlled Room Temperature] Manufactured by: Nexgen Pharma, Inc. Irvine, CA 92614 Distributed by: Breckenridge Pharmaceutical, Inc. Boca Raton, FL 33487 6920, 6921 Rev 11/08

PATIENT INFORMATION

SPL PATIENT PACKAGE INSERT SECTION

PATIENT INFORMATION Polyethylene Glycol 3350 NF (Polyethylene Glycol 3350 Powder for Oral Solution) is a prescription only laxative which has been prescribed by your physician to treat constipation. This product should only be used by the person for whom it was prescribed. How to take The dose is 17 grams each day or as directed by physician. It should always be taken by mouth. Measure the dose using the dosing cup (or use one heaping tablespoon of powder), stir and dissolve in a glass (4 to 8 oz) of water, juice, soda, coffee, or tea. Taking more than the prescribed dose may cause loss of fluid due to severe diarrhea. How will it work Polyethylene Glycol 3350 NF softens the stool and increases the frequency of bowel movements by retaining water in the stool. Your first bowel movement will usually happen in two to four days, although results may vary for individual patients. How long should I take it Polyethylene Glycol 3350 NF achieves its best results when used between one and two weeks. You may discontinue taking the drug after you had several satisfactory bowel movements. Should unusual cramps, bloating, or diarrhea occur, consult your physician. Polyethylene Glycol 3350 NF is intended for up to a two week course of therapy. You should not use for a longer time unless directed by your physician. Next Steps After successfully completing Polyethylene Glycol 3350 NF therapy (usually between one and two weeks), please discuss with your physician lifestyle changes which may produce more regular bowel habits (adequate dietary and fluid intake, regular exercise). Who should NOT take Polyethylene Glycol 3350 NF Polyethylene Glycol 3350 NF should not be used by children. It should not be used by pregnant women unless prescribed by a physician. Side Effects/Drug Reactions Occasionally, Polyethylene Glycol 3350 NF may cause nausea, stomach fullness, cramping, diarrhea and/or gas. Do not take if you have symptoms such as nausea, vomiting, abdominal pain or distention, which may be due to bowel obstruction. On rare occasions hives and skin rashes have been reported which are suggestive of an allergic reaction. If you get an allergic reaction you should discontinue the medication and call your physician. If you are allergic to polyethylene glycol, do not use this drug.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Source Document#

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