Ultravate Lotion
Product Images NDC 73159-008

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ultravate (NDC 73159-008). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lacer Pharma, 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

Carton Image (Ultravate Carton)

Packaging label for Ultravate 0.05% lotion containing halobetasol propionate. The label states the product is for topical use only, with a net content of 60 mL (59 g). The labeler is Lacer Pharma, LLC, and the NDC number is 73159-008-60. The label includes warnings for external use only and not for eye use, along with dosage instructions and ingredient details.*

FDA Label Image

Chemical Structure (Halobestasol 01)

Chemical structure diagram of halobetasol propionate, the active ingredient in ULTRAVATE topical lotion 0.5 mg/g by Lacer Pharma, LLC. The structure shows the steroid backbone with associated chlorine and fluorine atoms characteristic of this corticosteroid molecule.*

* 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.