Polyethylene Glycol 3350 Nf Powder, For Solution
Product Images NDC 11534-180

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Polyethylene Glycol 3350 Nf (NDC 11534-180). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sunrise Pharmaceutical, 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

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2ffddd92-figure-01 (2ffddd92 Figure 01)
Label for Polyethylene Glycol 3350 powder for solution, 17 g strength, an osmotic laxative by Sunrise Pharmaceutical, Inc. The label states it is unflavored, gluten-free, and designed to relieve occasional constipation by softening stool. The net weight is 4.1 oz (119 g), with dosing instructions and drug facts included. The product is made in the USA and intended for oral use.*
FDA Label Image

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2ffddd92-figure-02 (2ffddd92 Figure 02)
POLYETHYLENE GLYCOL 3350 powder for solution, osmotic laxative, 17 g strength by SUNRISE PHARMACEUTICAL, INC. Unflavored, grit-free powder in an 8.3 oz (238 g) container with 14 once-daily doses. The label highlights it as original prescription strength, relieves occasional constipation, softens stool, and dissolves in any beverage.*
FDA Label Image

2ffddd92-figure-03 (2ffddd92 Figure 03)

2ffddd92-figure-03 (2ffddd92 Figure 03)
Label for Polyethylene Glycol 3350 powder for solution, osmotic laxative, with original prescription strength. Contains 17.9 oz (510 g) in powder form, for oral use. The label states it relieves occasional constipation, softens stool, and dissolves in any beverage. Manufactured by Sunrise Pharmaceutical, Inc. The label includes Drug Facts with purpose, use, warnings, directions, inactive ingredients, and contact 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.