Betamethasone Dipropionate Ointment, Augmented
Product Images NDC 35573-107

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Betamethasone Dipropionate (NDC 35573-107). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Burel Pharmaceuticals, 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

Package Label.principal Display Panel (15 g Tube Label)

Package Label.principal Display Panel (15 g Tube Label)
Label for Betamethasone Dipropionate 0.05% ointment, USP (augmented), a topical prescription drug. The label states the product is for topical use only and comes in a 15 g tube. It is manufactured for Burel Pharmaceuticals, LLC and has an NDC of 35573-107-15. Additional information includes dosage instructions, storage conditions, and manufacturer details.*
FDA Label Image

Package Label.principal Display Panel (15 g Tube Carton Label)

Package Label.principal Display Panel (15 g Tube Carton Label)
The image shows the unfolded carton packaging label for Betamethasone Dipropionate Ointment, USP (Augmented) 0.05%, 15 g, a topical ointment. The label includes usage warnings, dosage information, storage conditions, and manufacturer details. It is labeled for prescription use only and manufactured for Burel Pharmaceuticals, LLC.*
FDA Label Image

Package Label.principal Display Panel (50 g Tube Label)

Package Label.principal Display Panel (50 g Tube Label)
Label for Betamethasone Dipropionate Ointment USP (Augmented) 0.05%, topical ointment, 50 g tube. The label includes usage instructions, storage conditions, manufacturer details (APL Health Care Limited, India) and labeler information (Burel Pharmaceuticals, LLC, Mason, OH). The packaging features the NDC 35573-107-49 and a barcode.*
FDA Label Image

Package Label.principal Display Panel (50 g Tube Carton Label)

Package Label.principal Display Panel (50 g Tube Carton Label)
The packaging label for Betamethasone Dipropionate 0.05% ointment, USP (Augmented), a topical prescription drug by Burel Pharmaceuticals, LLC. The 50 g carton displays strength as 0.05% betamethasone, usage instructions, storage conditions, and manufacturing details. It includes barcodes and a 2D data matrix area for batch and serial numbers.*
FDA Label Image

Str (Betamethasonestr)

Str (Betamethasonestr)
Chemical structure diagram of betamethasone dipropionate showing its molecular framework including fluorine, hydroxyl, acetate, and ketone functional groups.*

* 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.