Alclometasone Dipropionate Ointment
Product Images NDC 68462-299

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Alclometasone Dipropionate (NDC 68462-299). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Glenmark Pharmaceuticals 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

Cream-carton (Cream Carton)

Cream-carton (Cream Carton)
This is a product description for Alclometasone Dipropionate cream manufactured by Glenmark Pharmaceuticals Limited in India and Glenmark Pharmaceuticals Inc. in the USA. The cream is for dermatological use only and contains 0.05% of Alclometasone Dipropionate (HZEI) USP. The cream should be applied thinly to the affected skin areas two or three times a day. The usual dosage and prescription information can be found in the package insert. The cream should be stored between 2° and 30°C (36 and 86°F) to avoid freezing. The package is not child-resistant and should be kept out of reach of children. The packaging features an unvarnished area of 38mm x 20mm for the lot and expiry date. The National Drug Code (NDC) for the cream is 68462-300-47. If the metal tamper-resistant seal on the product has been punctured or is not visible, the product should not be used and returned to the place of purchase. Instructions on how to puncture the seal are included in the packaging.*
FDA Label Image
FDA Label Image

Ointment-carton (Ointment Carton)

Ointment-carton (Ointment Carton)
This is a description of a prescription medication called Alclometasone Dipropionate, made by Glenmark Pharmaceuticals. The medication is for dermatologic use only and should not be used for ophthalmic purposes. It comes in a package containing prescribing information, and the dosage is applied topically two or three times a day. The medication should be stored between 2°C and 30°C, and it should be kept out of reach of children. The National Drug Code (NDC) for this medication is 68462-299-47.*
FDA Label Image

Structure Formula

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