Desonide Cream
Product Images NDC 70771-1381

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Desonide (NDC 70771-1381). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences 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

Desonide Cream (B521d7c8 A5f4 43a0 979e 0035f6c2349f 02)

Label for Desonide Cream 0.05% topical cream by Zydus Pharmaceuticals. The label includes instructions for external use only, specifies a 15 g net weight, and notes prescription-only status. The label also features detailed composition and storage information, manufacturer details (Cadila Healthcare Ltd., Ahmedabad, India), and an NDC number 70771-1381-1.*

FDA Label Image

Desonide Cream (B521d7c8 A5f4 43a0 979e 0035f6c2349f 03)

Desonide Cream 0.05% topical cream packaging label showing product name, strength, and dosage form. The label states 'For external use only, not for ophthalmic use,' includes the NDC 70771-1381, and indicates a 15 g tube. The labeler is Zydus Lifesciences Limited (manufactured by Cadila Healthcare Ltd, India). A barcode and storage instructions at 20° to 25°C are also visible.*

* 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.