Desonide Lotion
Product Images NDC 62332-550

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Desonide (NDC 62332-550). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic 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

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Chemical structure diagram of desonide, the active ingredient in a topical lotion formulation. The structure shows a corticosteroid core with various functional groups attached, representing the molecular arrangement of desonide.*

FDA Label Image

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The image shows front and back labels for Desonide Lotion, 0.05% (0.5 mg/mL) topical lotion. The front label includes the product name, strength, NDC 62332-550-18, a note that it's for topical use only and not for ophthalmic use, volume 4 FL OZ (118 mL), and the Alembic Pharmaceuticals logo. The back label features usage instructions, active and inactive ingredients, storage conditions, manufacturer details (Alembic Pharmaceuticals Inc., New Jersey), a barcode, and placeholders for lot and expiry dates.*

FDA Label Image

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Desonide Lotion 0.05% topical lotion packaging label for a 4 fl oz (118 mL) bottle. The label indicates prescription use only and includes directions to shake well before use. It is manufactured by Alembic Pharmaceuticals Inc., with the NDC number 62332-550-18. The label lists inactive ingredients and storage instructions between 20° to 25°C. The design features blue and green accents with the Alembic logo.*

* 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.