Polyethylene Glycol 3350 Powder, For Solution
Product Images NDC 83324-002

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Polyethylene Glycol 3350 (NDC 83324-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chain Drug Marketing Association, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Polyethleneglcollabel1 (Polyethleneglcollabel1)

Polyethleneglcollabel1 (Polyethleneglcollabel1)
Label images for Polyethylene Glycol 3350 Oral Laxative Powder Solution show front and back panels. The front highlights the product name, active ingredient Polyethylene Glycol 3350, 17 g dose per serving, and net weight 238 g. The labeler is CHAIN DRUG MARKETING ASSOCIATION, INC., with 14 once-daily doses. The back label presents detailed Drug Facts and directions for use, cautionary statements, storage information, and a contact number for questions.*
FDA Label Image

Polyethleneglcollabel2 (Polyethleneglcollabel2)

Polyethleneglcollabel2 (Polyethleneglcollabel2)
Polyethylene Glycol 3350 oral laxative powder solution carton label by Chain Drug Marketing Association, Inc. The main panel shows the product name, active ingredient, dosage form, and strength (17 g per dose). It states it is an osmotic laxative for occasional constipation, unflavored, sugar-free, and grit-free, with 30 once-daily doses in an 18 oz (510 g) package. Additional panels display Drug Facts, usage directions, warnings, inactive ingredients, and manufacturer information.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.