Loteprednol Etabonate Suspension/ Drops
Product Images NDC 70244-034

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Loteprednol Etabonate (NDC 70244-034). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sentiss Pharmaceuticals Llc, 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

Chemical Structure (Image 01)

Chemical Structure (Image 01)
Chemical structure of Loteprednol Etabonate, showing its steroid backbone with characteristic functional groups and molecular formula indicated.*
FDA Label Image

5 mL Carton Label (Loteprednol Suspension 0.5 5 mL Carton.jpg)

5 mL Carton Label (Loteprednol Suspension 0.5 5 mL Carton.jpg)
Label for Loteprednol Etabonate Ophthalmic Suspension 0.5%, 5 mL bottle. The sterile ophthalmic suspension label shows it is for prescription use only, with storage instructions between 15° to 25°C and a warning not to freeze. The product is manufactured by Sentiss Pharmaceuticals LLC, San Clemente, CA, and also by a Swiss manufacturer. The label includes active ingredient details and a caution to shake vigorously before use.*
FDA Label Image

5 mL Container Label (Loteprednol Suspension 0.5 5 mL Container.jpg)

5 mL Container Label (Loteprednol Suspension 0.5 5 mL Container.jpg)
Loteprednol Etabonate Ophthalmic Suspension 0.5% (5 mg/mL) in a 5 mL ophthalmic drops bottle label by Sentiss Pharmaceuticals LLC. The label includes directions to shake vigorously before use and storage instructions, with the product manufactured in Switzerland and distributed by Sentiss Pharmaceuticals in California.*

* 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.