Betamethasone Valerate Aerosol, Foam
Product Images NDC 51672-4188

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Betamethasone Valerate (NDC 51672-4188). 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 of Betamethasone Valerate, a corticosteroid active ingredient, showing its steroid backbone with associated functional groups and ester side chain.*

FDA Label Image

Figure (Betamethasone 02)

An instructional illustration showing a person dispensing a foam product from an aerosol container onto the palm of their hand, depicting the proper method to apply a topical foam medication such as Betamethasone Valerate aerosol foam.*

FDA Label Image

Figure (Betamethasone 03)

An instructional illustration showing a person applying foam to their scalp using their hand. The image depicts topical administration of a foam product, consistent with topical medication application instructions.*

FDA Label Image

Figure (Betamethasone 04)

An instructional illustration showing a person rubbing their hands together with droplets above, indicating the action of applying or spreading a liquid or foam topically on the skin. No text or branding is visible.*

FDA Label Image

Figure (Betamethasone 05)

An instructional illustration showing a person washing hair under a showerhead with water. A black X over the image indicates that wetting the hair or scalp with water is not recommended.*

FDA Label Image

Principal Display Panel (50 g Can Carton)

Betamethasone Valerate 0.12% Foam topical aerosol carton label for dermatologic use by Sun Pharmaceutical Industries, Inc. The 50 g package includes dispensing instructions, warnings, and manufacturer information from Taro Pharmaceutical Industries Ltd.*

* 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.