Dexamethasone Sodium Phosphate 0.1% / Finasteride 0.1% / Minoxidil 5%
Product Images NDC 72934-4069

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% (NDC 72934-4069). 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.

FDA Label Image

Zc (8 End)

Label on a small amber glass bottle with a white cap, containing DEXAMETHASONE SODIUM PHOSPHATE 0.1% / FINASTERIDE 0.1% / MINOXIDIL 5% from Sincerus Florida, LLC. The label includes directions for use, storage instructions to keep at controlled room temperature (20-25°C), and contact information for reporting suspected adverse reactions, including a phone number and FDA website. The product is intended for external use only.*

FDA Label Image

Ds (4069 8 Front)

The image shows a brown glass bottle with a white child-resistant cap. The label indicates the product name as Dexamethasone Sodium Phosphate 0.1%, Finasteride 0.1%, and Minoxidil 5% solution, with a net content of 60 grams. The labeler is Sincerus Florida, LLC, and the product is marked as a compounded drug made in the USA. The NDC number 72934-4069 is partially visible on the label.*

FDA Label Image

Df (4069 8 Middle)

Brown glass bottle with a white screw cap containing DEXAMETHASONE SODIUM PHOSPHATE 0.1% / FINASTERIDE 0.1% / MINOXIDIL 5% solution. The label lists the active ingredients with their strengths and inactive ingredients, and shows a lot number and manufacturing date. 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.