Golytely Powder, For Solution
Product Images NDC 24338-236

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Golytely (NDC 24338-236). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Azurity Pharmaceuticals, 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

Base-label (Base Label)

Base-label (Base Label)
Instructions for Use for GoLYTELY (PEG-3350 and Electrolytes) powder for oral solution. The label includes important usage information such as mixing the powder with 4 liters of lukewarm water, drinking instructions, and precautions like not taking undissolved powder and avoiding solid foods before use. Manufacturer details note Azurity Pharmaceuticals, Inc.*
FDA Label Image

Polyethylene Glycol 3350 (Gol00 0002 01)

Polyethylene Glycol 3350 (Gol00 0002 01)
Chemical structure diagram of polyethylene glycol 3350, showing repeating ethylene glycol units with terminal hydroxyl groups.*
FDA Label Image

Sodium Sulfate (Gol00 0002 02)

Sodium Sulfate (Gol00 0002 02)
Chemical structure of sulfate ion, showing a sulfur atom centrally bonded to four oxygen atoms with two negative charges on two of the oxygen atoms.*
FDA Label Image

Sodium Bicarbonate (Gol00 0002 03)

Sodium Bicarbonate (Gol00 0002 03)
Chemical structure diagram of polyethylene glycol 3350 and associated ingredients in GoLYTELY, showing a molecular structure with sodium (Na+), oxygen, and carbon atoms arranged in a chain and ring formation typical for this polymer compound.*
FDA Label Image

Golytely-label (Golytely Label)

Golytely-label (Golytely Label)
GoLYTELY PEG-3350 and Electrolytes for Oral Solution powder label with detailed ingredient amounts for reconstitution to 4 liters. The label includes instructions to fill the bottle to the top line, NDC 24338-236-01, and states the product is manufactured for Azurity Pharmaceuticals, Inc. It lists powdered form amounts per jug: polyethylene glycol 236 g, sodium sulfate 22.74 g, sodium bicarbonate 6.74 g, sodium chloride 5.86 g, and potassium chloride 2.97 g.*

* 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.