Clobetasol Propionate Cream
Product Images NDC 68462-529

3 FDA label images from Glenmark Pharmaceutcials Inc., Usa · 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 Clobetasol Propionate (NDC 68462-529). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Glenmark Pharmaceutcials Inc., Usa, 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

Carton

Carton
The packaging label for Clobetasol Propionate Cream USP 0.05% displays the product name, strength, and dosage form prominently. It is a 15 g topical cream manufactured by Glenmark Pharmaceuticals Limited in India and labeled for Glenmark Pharmaceuticals Inc., USA. The label includes storage instructions, a tamper-resistant seal warning, and usage restrictions for dermatologic use only, not for ophthalmic use. The label also features barcodes and the NDC number 68462-529-17.*
FDA Label Image

Clobetasol-propionate-structure.jpg (Clobetasol Propionate Structure)

Clobetasol-propionate-structure.jpg (Clobetasol Propionate Structure)
Chemical structure diagram of clobetasol propionate, showing its molecular framework including chlorine, fluorine, hydroxyl, and ketone functional groups as part of its corticosteroid structure.*
FDA Label Image

Tube

Tube
Label for Clobetasol Propionate Cream USP 0.05%, topical cream with 0.5 mg/g strength, packaged in a 15 g size. The label states use for dermatologic use only and not for ophthalmic use. Manufactured by Glenmark Pharmaceuticals Limited, India, for Glenmark Pharmaceuticals Inc., USA. Includes storage instructions, warning to keep out of reach of children, and a barcode.*

* 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.