Betamethasone Dipropionate Usp, 0.05% Ointment
Product Images NDC 52817-824

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This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Betamethasone Dipropionate Usp, 0.05% (NDC 52817-824). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Trupharma 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.

Product Images & Figures Index

FDA Label Image

Carton-box (Carton Box)

Carton-box (Carton Box)
Betamethasone Dipropionate Ointment USP, 0.05% is a dermatologic medication for external use only. It should not be used on the eyes. Each gram of the product contains 0.64 mg of betamethasone. It is an ointment base of mineral oil and white petroleum. A thin layer of the ointment should be applied to the affected areas of the skin once or twice daily. The usual dosage, instructions for use, and other important information are provided in the package insert. The product is manufactured in Canada and distributed by Tasman Pharma Inc. in Westminster, PA. It is sealed with a metal tamper-resistant seal, and if this seal is broken or missing, the product should not be used.*
FDA Label Image

Chemical-structure (Chemical Structure)

Chemical-structure (Chemical Structure)
This is a chemical compound identified by its molecular formula and weight. Without further context, it is unclear what the compound is or what its properties are.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.