Betamethasone Dipropionate 0.05% / Minoxidil 5% / Niacinamide 2% / Pentoxifylline 0.5%
Product Images NDC 72934-4024

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% / Niacinamide 2% / Pentoxifylline 0.5% (NDC 72934-4024). 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

Sd (8 End)

Sd (8 End)
Brown glass bottle with a white child-resistant cap containing BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% / NIACINAMIDE 2% / PENTOXIFYLLINE 0.5%, labeled by Sincerus Florida, LLC. The label displays usage directions and contact information for adverse reactions, along with a QR code. The product is intended for topical application and external use only.*
FDA Label Image

Zc (4024 8 Front)

Zc (4024 8 Front)
The image shows a brown glass bottle with a white child-resistant cap containing BETAMETHASONE DIPROPIONATE 0.05%, MINOXIDIL 5%, NIACINAMIDE 2%, and PENTOXIFYLLINE 0.5% solution, 60gm. The label includes the NDC number 72934-4024-8 and identifies the labeler as Sincerus Florida, LLC. The product is marked as a compounded drug made in the USA.*
FDA Label Image

Fa (4024 8 Middle)

Fa (4024 8 Middle)
The image shows a brown glass bottle with a white cap containing BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% / NIACINAMIDE 2% / PENTOXIFYLLINE 0.5% solution. The label lists active ingredients with their USP percentages and inactive ingredients including Ethyl Alcohol USP and Propylene Glycol USP. The 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.