Clobetasol Propionate Ointment
Product Images NDC 16714-782

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Clobetasol Propionate (NDC 16714-782). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx Llc, 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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The text provides information about a product called Clobetasol Propionate Ointment USP, 0.05%, manufactured by Glenmark Pharmaceuticals Ltd. It contains information such as the product's dimensions, manufacturing location, and directions for use, including a warning to keep out of reach of children. It is meant for dermatological purposes only and should not be used for ophthalmic purposes. The text also includes the product's NDC code and the name of the manufacturer, Northstar Rx LLC.*

FDA Label Image

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FDA Label Image

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Clobetasol Propionate Ointment USP, 0.05% is a dermatological medication. It should not be used in the eye. The ointment base mainly consists of propylene glycol, sorbitan sesquioleate, and white petrolatum, while clobetasol propionate USP 0.05% is the active component. It should be kept out of reach of children, and the seal should not be punctured or visible when used. See package insert for complete prescribing information, including the lot number and expiration date. The medication should be stored at an optimal temperature between 20°C to 25°C (68°F to 77°F) with excursions allowed between 15°C to 30°C ( 59°F to 86°F) and should not be refrigerated. The manufacturer is NorthStar Healthcare and is manufactured by Glenmark Pharmaceuticals Limited in Himachal Pradesh, India. The expiration date is March 2018. Mfg. Lic. No.: MNB/05/182 Holdings UC.*

* 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.