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purelax drug information

POLYETHYLENE GLYCOL 3350
CVS Pharmacy · ORAL

Product NDC: 59779-306

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic namePOLYETHYLENE GLYCOL 3350
Labeler / manufacturerCVS Pharmacy
RouteORAL
Drug classOsmotic Laxative
Product NDC59779-306
Label effective date2026-09-02

Official product label reference

purelax — CVS Pharmacy

This page contains 15 source sections for POLYETHYLENE GLYCOL 3350, oral route. Label set 006a9eca-400f-47f5-bee5-facf7034043e, version 16.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Use • relieves occasional constipation (irregularity) • generally produces a bowel movement in 1 to 3 days

Purpose

Purpose Osmotic Laxative
Dosage and administration — label text
Directions • do not take more than directed unless advised by your doctor • the bottle top is a measuring cap marked to contain 17 grams of powder when filled to the indicated line (white section in cap) • adults and children 17 years of age and older: • use once a day • fill to top of white section in cap which is marked to indicate correct dose (17 g) • stir and dissolve in any 4 to 8 ounces of beverage (cold, hot or room temperature) then drink • do not combine with starch-based thickeners used for difficulty swallowing • ensure that the powder is fully dissolved before drinking • do not drink if there are any clumps • do not use no more than 7 days • children 16 years of age or under: ask a doctor
Warnings
Warnings Allergy alert: Do not use if you are allergic to polyethylene glycol Do not use if you have kidney disease, except under the advice and supervision of a doctor Ask a doctor before use if you have • nausea, vomiting or abdominal pain • a sudden change in bowel habits that lasts over 2 weeks • irritable bowel syndrome Ask a doctor or pharmacist before use if you are taking a prescription drug When using this product you may have loose, watery, more frequent stools Stop use and ask a doctor if • you have rectal bleeding or your nausea, bloating, cramping or abdominal pain gets worse. These may be signs of a serious condition. • you get diarrhea • you need to use a laxative for longer than 1 week If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Active ingredient
Active ingredient (in each dose) Polyethylene Glycol 3350, 17 g (cap filled to line)
Do not use
Do not use if you have kidney disease, except under the advice and supervision of a doctor
Ask a doctor before use
Ask a doctor before use if you have • nausea, vomiting or abdominal pain • a sudden change in bowel habits that lasts over 2 weeks • irritable bowel syndrome
Ask a doctor or pharmacist
Ask a doctor or pharmacist before use if you are taking a prescription drug
While using this medicine
When using this product you may have loose, watery, more frequent stools
When to stop use and seek help
Stop use and ask a doctor if • you have rectal bleeding or your nausea, bloating, cramping or abdominal pain gets worse. These may be signs of a serious condition. • you get diarrhea • you need to use a laxative for longer than 1 week
Pregnancy or breast feeding
If pregnant or breast-feeding, ask a health professional before use.
Child safety
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Storage and handling
Other information • store at 20˚-25˚C (68˚-77˚F) • tamper-evident: do not use if printed foil seal under cap is missing, open or broken
Inactive ingredient
Inactive ingredients none
Questions
Questions or comments? 1-800-719-9260

Official sources and product identifiers

Substances listed: POLYETHYLENE GLYCOL 3350

RxNorm identifiers: 1010732, 876193

Package NDC codes

59779-306-01, 59779-306-02, 59779-306-03, 59779-306-04, 59779-306-53, 59779-306-18, 59779-306-17, 59779-306-19, 59779-306-52, 59779-306-60, 59779-306-09

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.