Betamethasone Dipropionate Lotion, Augmented
Product Images NDC 51672-1340

2 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Betamethasone Dipropionate (NDC 51672-1340). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Chemical Structure (Betamethasone 01)

Chemical Structure (Betamethasone 01)
Chemical structure diagram of Betamethasone Dipropionate, showing its molecular framework with labeled functional groups and atoms.*
FDA Label Image

Principal Display Panel (30 mL Bottle Carton)

Principal Display Panel (30 mL Bottle Carton)
Betamethasone Dipropionate Lotion (Augmented) USP 0.05% 30 mL carton label. The label includes active ingredient strength, usage warnings (for dermatologic use only, not ophthalmic), storage instructions, and manufacturer information from Taro Pharmaceuticals. It also displays the product NDC 51672-1340-3, and indicates prescription use only (Rx only).*

* 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.