Desonide Ointment
Product Images NDC 46708-485

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 Desonide (NDC 46708-485). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals Limited, 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

Structure (98a69c58 33de 41e1 A26f 7a4152605f05 01)

Structure (98a69c58 33de 41e1 A26f 7a4152605f05 01)
Chemical structure diagram of desonide, showing its steroid-based molecular framework with multiple rings, hydroxyl groups, and ester functional groups.*
FDA Label Image

Tube Image (98a69c58 33de 41e1 A26f 7a4152605f05 02)

Tube Image (98a69c58 33de 41e1 A26f 7a4152605f05 02)
Label for Desonide Ointment, 0.05% (equivalent to 0.5 mg/g), topical ointment by Alembic Pharmaceuticals Limited. The label specifies external use only, a net weight of 15 grams, and includes a barcode, NDC 46708-485-15, along with storage and usage instructions. It features color bars in blue (Pantone 285 C), green (Pantone 362 C), and black.*
FDA Label Image

Carton Image (98a69c58 33de 41e1 A26f 7a4152605f05 03)

Carton Image (98a69c58 33de 41e1 A26f 7a4152605f05 03)
Desonide Ointment 0.05% topical ointment packaging carton label displays the active ingredient strength as 0.5 mg/g. The label includes instructions for external use only and has warnings against ophthalmic use. It shows a net weight of 15 grams and is manufactured by Alembic Pharmaceuticals Limited. The label features the NDC number 46708-485-15 and includes barcode and batch coding areas.*

* 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.