Polyethylene Glycol 3350, Nf Powder For Solution, Laxative
Product Images NDC 0722-7116

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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 Powder For Solution, Laxative (NDC 0722-7116). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nexgen Pharma, 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

Nexgen Peg Otc 119g

Nexgen Peg Otc 119g
Label for Nexgen Polyethylene Glycol 3350, NF Powder for Solution, Laxative. It specifies original prescription strength, dissolves in any beverage, relieves occasional constipation, softens stool, and contains 7 once-daily doses with a net weight of 4.1 oz (119 g). Manufactured by Nexgen Pharma, Inc., Irvine, CA.*
FDA Label Image

Nexgen Peg Otc 238g

Nexgen Peg Otc 238g
Drug Facts panel for Nexgen Polyethylene Glycol 3350, NF Powder for Solution, Laxative. Includes active ingredient (Polyethylene Glycol 3350, 17g per dose), use instructions, warnings, directions, and storage information. Indicates it relieves occasional constipation and softens stool. Provides contact info for Nexgen Pharma, Inc., Irvine, CA, and includes warnings for allergies, kidney disease, and when to consult a doctor.*
FDA Label Image

Nexgen Peg Otc 510g

Nexgen Peg Otc 510g
Drug Facts label for Nexgen Polyethylene Glycol 3350, NF Powder for Solution, Laxative, 17.9 oz (510 g) with 30 once-daily doses. Provides directions, warnings, inactive ingredient information, storage conditions, and contact info. Highlights relief of occasional constipation and stool softening with 17 g polyethylene glycol 3350 per dose.*

* 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.