Gavilyte-n Powder, For Solution
Product Images NDC 43386-050

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Gavilyte-n (NDC 43386-050). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin 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

Peg Structure (3ff4d772 6527 4791 9236 E1a97878a200 01)

Chemical structure of polyethylene glycol-3350, showing the repeating ethylene glycol units with terminal hydroxyl groups represented in a simplified polymer notation.*

FDA Label Image

Sod-bicarbonate (3ff4d772 6527 4791 9236 E1a97878a200 02)

Chemical structure of sodium bicarbonate, showing the arrangement of sodium, carbon, oxygen, and hydrogen atoms.*

FDA Label Image

Label (3ff4d772 6527 4791 9236 E1a97878a200 03)

GaviLyte™-N powder for solution with flavor pack containing polyethylene glycol 3350, sodium bicarbonate, sodium chloride, and potassium chloride for oral solution. Label includes medication preparation instructions, active ingredient quantities, and manufacturer Lupin Pharmaceuticals, Inc. The package design features a green panel with product name and detailed directions for use.*

FDA Label Image

Flavor Packs (3ff4d772 6527 4791 9236 E1a97878a200 04)

Three flavor pack labels for GAVILYTE-N powder for solution with flavors: Lemon, Orange, and Cherry. Each label states it is to be pre-mixed with PEG-3350 and Electrolytes Powder for Oral Solution before dispensing and is for use only in combination with the accompanying container. Each pack has a net weight of 2 g and is labeled by Lupin Pharmaceuticals.*

* 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.