Loteprednol Etabonate Suspension/ Drops
Product Images NDC 62756-232

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Loteprednol Etabonate (NDC 62756-232). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Spl-loteprednol-carton (Spl Loteprednol Carton)

Loteprednol Etabonate Ophthalmic Suspension 0.5% in a 5 mL bottle, distributed by Sun Pharmaceutical Industries, Inc. and manufactured by Sun Pharmaceutical Medicare Ltd. The label includes active ingredient concentration, preservative details, storage instructions, barcode, and a statement to shake vigorously before use. The product is for ophthalmic use only and is prescription sterile.*

FDA Label Image

Spl-loteprednol-label (Spl Loteprednol Label)

Loteprednol Etabonate 0.5% ophthalmic suspension eye drops in a 5 mL bottle. Label indicates the product is sterile, for prescription use only, and instructs to shake vigorously before use. Each milliliter contains 5 mg of Loteprednol Etabonate. Storage instructions specify to keep the product upright between 20°C and 25°C (68°F to 77°F) and not to freeze. Distributed by Sun Pharmaceutical Industries, Inc., New Jersey, and manufactured by Sun Pharmaceutical Medicare Ltd., India.*

FDA Label Image

Spl-loteprednol-structure (Spl Loteprednol Structure)

Chemical structure diagram of Loteprednol Etabonate, showing its molecular composition including hydroxyl, methyl, oxygen, chloro, and ketone groups arranged in its corticosteroid framework.*

* 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.