Androgel
Product Images NDC 17139-501

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Androgel (NDC 17139-501). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ascend Therapeutics U.s., 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

Ndc 17139-525-30 (17139 525 30)

Ndc 17139-525-30 (17139 525 30)
Label for AndroGel testosterone gel 1%, containing 25 mg of testosterone per 2.5 grams of gel. The label indicates topical use only, is marked Rx only, and includes warnings about flammability and keeping out of reach of children. Manufactured by ASCEND Therapeutics U.S., LLC.*
FDA Label Image

Ndc 17139-550-30 (17139 550 30)

Ndc 17139-550-30 (17139 550 30)
AndroGel 1% testosterone gel packaging label showing it contains 50 mg of testosterone per 5 grams of gel for topical use. Marketed by ASCEND Therapeutics U.S., LLC, the label includes a warning about the gel being alcohol-based and flammable, advising to avoid fire, flame, or smoking until the gel has dried. The label also directs users to read the medication guide and indicates Rx only.*
FDA Label Image

Figure 1 (Androgel 1 Figure 1)

Figure 1 (Androgel 1 Figure 1)
A line graph showing testosterone concentration (ng/dL) over time (hours) after application for AndroGel 5 g and 10 g doses. The graph compares concentration levels at various time points, with lines representing both dose levels and markers for high and low normal concentrations.*
FDA Label Image

Figure 2 (Androgel 1 Figure 2)

Figure 2 (Androgel 1 Figure 2)
A line graph depicting the testosterone concentration (ng/dL) over 24 hours after application of AndroGel at 5 g and 10 g doses. The graph shows testosterone levels measured on Day 30, Day 90, and Day 180, with upper and lower limits of the normal range indicated for comparison.*
FDA Label Image

Figure A (Androgel 1 Figure A)

Figure A (Androgel 1 Figure A)
An instructional diagram showing recommended application sites on the human body for AndroGel. The highlighted areas include both shoulders and the front torso, indicating where the gel should be applied. The illustration includes front and side views of a male figure to demonstrate application locations.*
FDA Label Image

Front View (Androgel 1 Front View)

Front View (Androgel 1 Front View)
An illustration showing a male torso with highlighted areas on both shoulders and the central chest and abdomen. This diagram likely indicates application sites for a topical product like AndroGel.*
FDA Label Image

Side View (Androgel 1 Side View)

Side View (Androgel 1 Side View)
An illustration depicting the front upper body of a person with shaded areas on the left shoulder and left abdomen, indicating application sites for a topical product.*
FDA Label Image

Structural Formula (Androgel 1 Structural)

Structural Formula (Androgel 1 Structural)
Chemical structure of testosterone, displaying its molecular arrangement with the formula C19H28O2 and molecular weight 288.42. The image includes the label "Testosterone" underneath the structure, and depicts typical steroid rings and functional groups.*
FDA Label Image

Ndc 17139-501-02 (Pump Label)

Ndc 17139-501-02 (Pump Label)
AndroGel 1.62% (testosterone gel) metered pump label from ASCEND Therapeutics U.S., LLC. The label indicates each pump activation delivers 20.25 mg testosterone and specifies usage instructions for topical application. The label includes dosing information with a table of testosterone amounts per number of pump activations, and highlights Rx only status.*

* 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.