Pramosone Ointment
Product Images NDC 54766-777

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pramosone (NDC 54766-777). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sebela Pharmaceuticals Inc., 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

Hydrocortisoneacetate (Pramosone Figure 1)

FDA Label Image

Pramointment2.5rev1212 (Pramosone Figure 2)

This is a medication called Pramosone®. It is an ointment with hydrocortisone acetate 2.5% and pramoxine HCl 1%, used for external use only. The ointment is paraben-free and should be applied to the affected area 3-4 times a day. The medication should be stored at 25°C (77°F), and the tube crimp should be checked for the Lot No. and expiration date. The medication is manufactured for Sebela Ireland Ltd. by Ferndale Laboratories, Inc. and distributed by Sebela Pharmaceuticals Inc. The contact information for Sebela Pharmaceuticals Inc. is provided.*

FDA Label Image

Pramoxinehcl (Pramosone Figure 3)

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