COMFORTLAX
COMFORTLAX is an FDA drug label for the active ingredient POLYETHYLENE GLYCOL 3350 manufactured by Family Dollar Stores, LLC administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260423.
- Generic name
- POLYETHYLENE GLYCOL 3350
- Manufacturer
- Family Dollar Stores, LLC
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 55319-056
- Application
- ANDA209017
- Label effective
- 20260423
About this product
COMFORTLAX is an FDA-registered drug product whose active ingredient is POLYETHYLENE GLYCOL 3350. It is labelled by Family Dollar Stores, LLC taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 55319-056, application ANDA209017, label effective 20260423. It is one of 45 FDA drug label records sharing the active ingredient POLYETHYLENE GLYCOL 3350. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing POLYETHYLENE GLYCOL 3350 are most often described in connection with: relieves occasional, constipation irregularity, generally produces, bowel movement. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use relieves occasional constipation (irregularity) generally produces a bowel movement in 1 to 3 days
Dosage & Administration
Directions do not take more than directed unless advised by your doctor this product is supplied with a dosing cup marked to contain 17 grams of powder when filled to the indicated line adults and children 17 years of age and older: use once a day fill to the indicated 17 grams line on cup which is marked to indicate the correct dose 17 grams 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
More products with the same ingredient
POLYETHYLENE GLYCOL 3350365 WHOLE FOODS MARKET Polyethylene Glycol 3350
View labelCLEARLAX
View labelCLEARLAX
View labelCLEARLAX
View labelEquate ClearLAX
View labelGAVILAX
View labelGAVILAX
View labelHow products containing POLYETHYLENE GLYCOL 3350 compare
FDA lists 45 drug label records with POLYETHYLENE GLYCOL 3350 as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Amazon.com Services LLC | 4 |
| — | — | L. Perrigo Company | 3 |
| — | — | CVS Pharmacy | 2 |
| — | — | Cardinal Health 107, LLC | 2 |
| — | — | Major Pharmaceuticals | 2 |
Recall and safety notices
5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-0566-2023 | Advil Liqui-Gels Solubilized Ibuprofen Capsules, 200 mg Pain Reliever/Fever Reducer (NSAID) a) 20-count Liquid Filled Capsule bottles; b) 40-count Liquid Filled Capsule bottles. | Family Dollar Stores, Llc. | Class II | Ongoing | 20230510 |
| D-0565-2023 | Advil Dual Action with Acetaminophen Acetaminophen 250 mg and Ibuprofen (NSAID) 125 mg Tablets Pain Reliever, 36 Caplets bottles | Family Dollar Stores, Llc. | Class II | Ongoing | 20230510 |
| D-0564-2023 | Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) 24-count Caplets | Family Dollar Stores, Llc. | Class II | Ongoing | 20230510 |
| D-0563-2023 | Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) packaged in a) 100-count bottles, b) 50-count bottles, and c) 3 (2 count) packets. | Family Dollar Stores, Llc. | Class II | Ongoing | 20230510 |
| D-1465-2022 | Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES, Stain Prevention, 5% Hydrogen Peroxide, Net Wt. 2.1 OZ. (59 g) UPC 0 35000 99658 9. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A. | Family Dollar Stores, Llc. | Class II | Ongoing | 20220907 |
Frequently asked questions
What is COMFORTLAX used for?
Use relieves occasional constipation (irregularity) generally produces a bowel movement in 1 to 3 days
Who makes COMFORTLAX?
Family Dollar Stores, LLC is the labeler of record for COMFORTLAX. 45 FDA label records share the active ingredient POLYETHYLENE GLYCOL 3350, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does COMFORTLAX come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is COMFORTLAX prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Are there other products containing POLYETHYLENE GLYCOL 3350?
Yes. 45 FDA drug label records list POLYETHYLENE GLYCOL 3350 as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has COMFORTLAX been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.