Dexamethasone Sodium Phosphate 0.1% / Finasteride 0.1% / Minoxidil 5% / Tretinoin 0.025%
Product Images NDC 72934-4070

3 FDA label images from Sincerus Florida · 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 Dexamethasone Sodium Phosphate 0.1% / Finasteride 0.1% / Minoxidil 5% / Tretinoin 0.025% (NDC 72934-4070). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florida, 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

Ed (8 End)

Ed (8 End)
Dexamethasone Sodium Phosphate 0.1% / Finasteride 0.1% / Minoxidil 5% / Tretinoin 0.025% in a brown glass bottle with a white screw cap. The visible label includes usage directions and contact information for Sincerus Florida, LLC, the labeler located in Pompano Beach, FL.*
FDA Label Image

Zc (4070 8 Front)

Zc (4070 8 Front)
Amber glass bottle with a white cap containing a compounded drug solution. The label lists active ingredients as Dexamethasone Sodium Phosphate USP 0.1%, Finasteride USP 0.1%, Minoxidil USP 5%, and Tretinoin USP 0.025%, in a 60gm solution. The label displays NDC 72934-4070-8 and the Sincerus Florida logo, indicating the labeler.*
FDA Label Image

Sd (4070 8 Middle)

Sd (4070 8 Middle)
The image shows a brown pharmaceutical bottle with a white ribbed cap, featuring a label listing active and inactive ingredients. The label specifies Dexamethasone Sodium Phosphate 0.1%, Finasteride USP 0.1%, Minoxidil USP 5%, and Tretinoin USP 0.025% as active ingredients. The product is labeled under Sincerus Florida with NDC 72934-4070.*

* 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.