Propecia
Product Images NDC 54868-4120

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Propecia (NDC 54868-4120). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, Inc., 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

Package Label (4120)

Label for PROPECIA 1 MG tablets distributed by Physicians Total Care, Inc. The label includes the product name, dosage strength of 1 mg, a lot number (0000), expiration date (01/60), and a barcode. The package contains 30 tablets.*

FDA Label Image

Image Of Finasteride Chemical Structure (Propecia 01)

Chemical structure of the active ingredient in PROPECIA, showing a steroidal framework with specific functional groups including a keto group and an amide side chain with a tert-butyl substituent.*

FDA Label Image

Image Of Figure 1 (Propecia 02)

A line graph titled 'Effect on Hair Count' showing the mean change in the number of hairs in a 1-inch diameter circle over time with standard error bars. The x-axis represents time in months and years, while the y-axis shows the mean change from baseline in hair count. Four groups are plotted, including finasteride 1 mg and placebo, with sample sizes decreasing over time. The data are pooled from vertex hair loss studies.*

FDA Label Image

Principal Display Panel (1 mg Bottle Label)

Propecia 1 mg (finasteride) Tablets label showing the product name, active ingredient and strength, bottle count of 30 tablets, and warnings about use for women and children. The label includes storage instructions and manufacturer details, with a barcode and an image of a single peach-colored tablet marked PROPECIA.*

* 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.