Betamethasone Dipropionate 0.05% / Minoxidil 5%
Product Images NDC 72934-4023

3 FDA label images from Sincerus Florida, 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 0.05% / Minoxidil 5% (NDC 72934-4023). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florida, 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.

Product Images & Figures Index

FDA Label Image

E (4023 8 End)

E (4023 8 End)
Text panel provides directions for use of the product by Sincerus Florida, LLC, instructing application as directed by a physician, topical use only, hand washing after use, and storage at controlled room temperature (20-25°C). Includes contact information for reporting adverse reactions and a QR code.*
FDA Label Image

X (4023 8 Front)

X (4023 8 Front)
Betamethasone Dipropionate 0.05% / Minoxidil 5% solution in a 60gm amber bottle with a white child-resistant cap. The label includes the NDC 72934-4023-8 and indicates it is a compounded drug made in the USA by Sincerus Florida, LLC. The label prominently displays the brand name Sincerus Florida with a blue and orange logo.*
FDA Label Image

X (4023 8 Middle)

X (4023 8 Middle)
Brown medicine bottle with white cap labeled BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% solution. Label includes active ingredients Betamethasone Dipropionate USP 0.05% and Minoxidil USP 5%, along with inactive ingredients Ethyl Alcohol USP and Propylene Glycol USP. Product is marked Rx only and includes manufacture and expiration dates. Labeler is Sincerus Florida, LLC.*

* 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.