Betamethasone Dipropionate Lotion, Augmented
Product Images NDC 0168-0267

3 FDA label images from E. Fougera & Co. A Division Of Fougera Pharmaceuticals, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Betamethasone Dipropionate (NDC 0168-0267). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by E. Fougera & Co. A Division Of Fougera 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

Chemical Structure (Image 01)

Chemical Structure (Image 01)
Chemical structure of betamethasone dipropionate, the active ingredient in the topical lotion form of this human prescription drug.*
FDA Label Image

Principal Display Panel 30ml Label (Image 02)

Principal Display Panel 30ml Label (Image 02)
Label for Betamethasone Dipropionate Lotion USP (Augmented) 0.05% topical lotion, 30 mL, from E. Fougera & Co. It specifies prescription use only, storage instructions at 20-25°C with allowed excursions, and cautions against oral, ophthalmic, or intravaginal use. Includes ingredients, manufacturer details, and a barcode.*
FDA Label Image

Principal Display Panel 30ml Ctn (Image 03)

Principal Display Panel 30ml Ctn (Image 03)
Packaging label for Betamethasone Dipropionate Lotion USP (Augmented) 0.05%, a topical prescription lotion. The 30 mL container label is yellow and white and produced by E. Fougera & Co., a division of Fougera Pharmaceuticals, LLC. The label includes usage warnings, storage instructions, and lists ingredients including 0.643 mg betamethasone dipropionate per gram.*

* 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.