Polyethylene Glycol 3350 Powder, For Solution
Product Images NDC 73581-913

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Polyethylene Glycol 3350 (NDC 73581-913). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Yyba Corp, 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

Carton (Peg Carton)

Carton (Peg Carton)
Polyethylene Glycol 3350 osmotic powder to solution laxative in 17 g single-serve packets. The box contains 40 packets and is labeled as unflavored, grit free, travel ready, and sugar free. The labeler is YYBA Corp. The packaging highlights occasional constipation relief and bowel movement frequency increase.*
FDA Label Image

Label1 (Peg Label 1)

Label1 (Peg Label 1)
Packaging label for Welmate Laxative osmotic powder to solution containing Polyethylene Glycol 3350. The powder is unflavored, grit-free, and contains no added sugar. The net weight is 0.5 oz (17 g), with 40 individually wrapped single-serve doses. The label highlights relief for occasional constipation and irregularity, softening stool, and increasing bowel movement frequency. Manufactured by YYBA Corp.*
FDA Label Image

Label2 (Peg Label 2)

Label2 (Peg Label 2)
Drug Facts label for Polyethylene Glycol 3350 oral powder, 17 g per dose, describes its use as an osmotic laxative to relieve occasional constipation. The label includes warnings, directions for use, storage instructions, inactive ingredients, and contact information, along with cautions for specific medical conditions and usage limitations.*

* 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.