Hydrocortisone Valerate Ointment
Product Images NDC 51672-1292

3 FDA label images from Sun Pharmaceutical Industries, Inc. · 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 Hydrocortisone Valerate (NDC 51672-1292). 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 (Hydrocortisone 01)

Chemical Structure (Hydrocortisone 01)
Chemical structure of hydrocortisone valerate. The image depicts the molecular structure with its characteristic steroid backbone and ester group, consistent with the active ingredient hydrocortisone valerate.*
FDA Label Image

Principal Display Panel (45 g Tube Carton)

Principal Display Panel (45 g Tube Carton)
Packaging label for Hydrocortisone Valerate Cream USP 0.2%, topical ointment in a 15 g tube. The label includes directions, storage instructions, and manufacturer information for Taro Pharmaceuticals. The product is indicated for dermatologic use only and is labeled Rx only.*
FDA Label Image

Principal Display Panel (45 g Tube Carton)

Principal Display Panel (45 g Tube Carton)
Packaging label for Hydrocortisone Valerate ointment USP 0.2%, topical dosage form, containing 2 mg/g hydrocortisone valerate in a 15 g tube. The label shows the product name, strength, and form, directions for use, storage instructions, manufacturer as Taro Pharmaceutical Industries Ltd., and distributor Taro Pharmaceuticals U.S.A., Inc. The label includes warnings and a barcode.*

* 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.