Polyethylene Glycol 3350 Powder, For Solution
Product Images NDC 68001-607

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Polyethylene Glycol 3350 (NDC 68001-607). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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

510g Front Label (510g Label Page 1 Rev 06 23)

Label for Polyethylene Glycol 3350 Powder for Oral Solution 17 g/dose by BluePoint Laboratories. It is an osmotic laxative in powder form, unflavored and grit-free, providing 30 once-daily doses with a net weight of 17.9 oz (510 g). The label includes drug facts and usage instructions on the top layer back and second layer panels.*

FDA Label Image

510g Back Label (510g Label Page 2 Rev 06 23)

Packaging label for Polyethylene Glycol 3350 powder for oral solution by BluePoint Laboratories. The label includes product use instructions, drug facts, inactive ingredients, manufacturer information, and barcode. It highlights the product dissolves in any beverage and is sugar-free. The label also features layering instructions and measurements for the printed label.*

FDA Label Image

Bottlelabelfront (Polythylene Glycol Powder For Oral Solution 238g Label Page 1 Rev 06 23)

Polyethylene Glycol 3350 Powder for Oral Solution, 17 g per dose, osmotic laxative by BluePoint Laboratories. Front label shows 14 once-daily doses, unflavored and grit-free powder. Included is detailed Drug Facts information on active ingredient, uses, warnings, and precautions covering occasional constipation and laxative use.*

FDA Label Image

Bottlebacklabel (Polythylene Glycol Powder For Oral Solution 238g Label Page 2 Rev 06 23)

Drug Facts panels for Polyethylene Glycol 3350 powder for oral solution by BluePoint Laboratories. The text includes usage directions, overdose instructions, storage conditions, inactive ingredients, and contact information. The labeling format details font types and sizes used for different text elements on the label.*

* 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.