Patient information: uses, side effects, how to take - Androgel Topical 16.2 mg/g

What is the most important information I should know about ANDROGEL 1.62%?

1. ANDROGEL 1.62% can transfer from your body to others including, children and women. Children and women should avoid contact with the unwashed or not covered (unclothed) areas where ANDROGEL 1.62% has been applied to your skin. Early signs and symptoms of puberty have occurred in young children who have come in direct contact with testosterone by touching areas where men have used ANDROGEL 1.62%.

Children

Signs and symptoms of early puberty in a child when they come in direct contact with ANDROGEL 1.62% may include:

Abnormal sexual changes:

enlarged penis or clitoris.
early growth of hair near the vagina or around the penis (pubic hair).
erections or acting out sexual urges (sex drive).

Behavior problems:

acting aggressively, behaving in an angry or violent way.

Women

Signs and symptoms in women when they come in direct contact with ANDROGEL 1.62% may include:

changes in body hair.
an abnormal increase in pimples (acne).

Stop using ANDROGEL 1.62% and call your healthcare provider right away if you see any signs and symptoms in a child or a woman that may have happened through accidental touching of the area where you have applied ANDROGEL 1.62%.

2. To lower the risk of transfer of ANDROGEL 1.62% from your body to others, follow these important instructions:

Apply ANDROGEL 1.62% only to your shoulders and upper arms that will be covered by a short sleeve t-shirt.
Wash your hands right away with soap and water after applying ANDROGEL 1.62%.
After the gel has dried, cover the application area with clothing. Keep the area covered until you have washed the application area well or have showered.
If you expect to have skin-to-skin contact with another person, first wash the application area well with soap and water.
If a child or woman touches the area where you have applied ANDROGEL 1.62%, that area on the child or woman should be washed well with soap and water right away.

What is ANDROGEL 1.62%?

ANDROGEL 1.62% is a prescription medicine that contains testosterone. ANDROGEL 1.62% is used to treat adult males who have low or no testosterone due to certain medical conditions.

Your healthcare provider will test your blood before you start and while you are using ANDROGEL 1.62%.
It is not known if ANDROGEL 1.62% is safe or effective to treat men who have low testosterone due to aging.
It is not known if ANDROGEL 1.62% is safe or effective in children younger than 18 years old. Improper use of ANDROGEL 1.62% may affect bone growth in children.

ANDROGEL 1.62% is a controlled substance (CIII) because it contains testosterone that can be a target for people who abuse prescription medicines. Keep your ANDROGEL 1.62% in a safe place to protect it. Never give your ANDROGEL 1.62% to anyone else, even if they have the same symptoms you have. Selling or giving away this medicine may harm others and is against the law.

ANDROGEL 1.62% is not meant for use in women.

Do not use ANDROGEL 1.62% if you:

have breast cancer.
have or might have prostate cancer.
are pregnant. ANDROGEL 1.62% may harm your unborn baby.
Women who are pregnant should avoid contact with the area of skin where ANDROGEL 1.62% has been applied.

Before using ANDROGEL 1.62%, tell your healthcare provider about all of your medical conditions, including if you:

have breast cancer.
have or might have prostate cancer.
have urinary problems due to an enlarged prostate.
have heart problems.
have high blood pressure or are being treated for high blood pressure.
have kidney or liver problems.
have problems breathing while you sleep (sleep apnea).

Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Using ANDROGEL 1.62% with certain other medicines can affect each other.

Especially, tell your healthcare provider if you take:

insulin
medicines that decrease blood clotting (blood thinners)
corticosteroids

How should I use ANDROGEL 1.62%?

See the detailed Instructions for Use about how to use ANDROGEL 1.62% at the end of this Medication Guide.
It is important that you apply ANDROGEL 1.62% exactly as your healthcare provider tells you to.
Your healthcare provider may change your ANDROGEL 1.62% dose. Do not change your ANDROGEL 1.62% dose without talking to your healthcare provider.
Apply ANDROGEL 1.62% at the same time each morning. ANDROGEL 1.62% should be applied after showering or bathing.

What are the possible side effects of ANDROGEL 1.62%?

ANDROGEL 1.62% can cause serious side effects including:

See “What is the most important information I should know about ANDROGEL 1.62%?”

If you already have enlargement of your prostate gland your signs and symptoms can get worse while using ANDROGEL 1.62%. This can include:
○ increased urination at night.
○ trouble starting your urine stream.
○ having to pass urine many times during the day.
○ having an urge to go to the bathroom right away.
○ having a urine accident.
○ being unable to pass urine or weak urine flow.
Possible increased risk of prostate cancer. Your healthcare provider should check you for prostate cancer or any other prostate problems before you start and while you use ANDROGEL 1.62%.
Blood clots in the legs or lungs. Signs and symptoms of a blood clot in your leg can include leg pain, swelling, or redness. Signs and symptoms of a blood clot in your lungs can include difficulty breathing or chest pain.
Increase in blood pressure. AndroGel 1.62% can increase your blood pressure. Increases in blood pressure can increase the risk of heart attack or stroke over time. If your blood pressure increases while on AndroGel 1.62%, blood pressure medicines may need to be started. If you are taking blood pressure medicines, new blood pressure medicines may need to be added or your current blood pressure medicines may need to be adjusted to control your blood pressure. If your blood pressure cannot be controlled, AndroGel 1.62% may need to be stopped. Your healthcare provider will monitor your blood pressure while you are being treated with AndroGel 1.62%.
In large doses ANDROGEL 1.62% may lower your sperm count.
Swelling of your ankles, feet, or body, with or without heart failure.
Enlarged or painful breasts.
Have problems breathing while you sleep (sleep apnea).

Call your healthcare provider right away if you have any of the serious side effects listed above.

The most common side effects of ANDROGEL 1.62% include:

increased prostate specific antigen (a test used to screen for prostate cancer)
mood swings
hypertension
increased red blood cell count
skin irritation where ANDROGEL 1.62% is applied

Other side effects include more erections than are normal for you or erections that last a long time.

Tell your healthcare provider if you have any side effect that bothers you or that does not go away.

These are not all the possible side effects of ANDROGEL 1.62%. For more information, ask your healthcare provider or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

General information about the safe and effective use of ANDROGEL 1.62%

Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use ANDROGEL 1.62% for a condition for which it was not prescribed. Do not give ANDROGEL 1.62% to other people, even if they have the same symptoms you have. It may harm them. You can ask your pharmacist or healthcare provider for information about ANDROGEL 1.62% that is written for health professionals.

What are the ingredients in ANDROGEL 1.62%?

Active ingredient: testosterone

Inactive ingredients: carbopol 980, ethyl alcohol, isopropyl myristate, purified water and sodium hydroxide.

For more information about ANDROGEL 1.62%, call 1-877-204-1013 or go to www.androgel.com.

This Medication Guide has been approved by the U.S. Food and Drug Administration Revised: 07/2025

2025AG0003

INSTRUCTIONS FOR USE

ANDROGEL^®(AN DROW JEL) CIII

(testosterone gel) 1.62%

for topical use

Read this Instructions for Use for ANDROGEL1.62% before you start using it and each time you get a refill. There may be new information. This leaflet does not take the place of talking to your healthcare provider about your medical condition or treatment.

Applying ANDROGEL 1.62%:

ANDROGEL 1.62% comes in a pump or in packets.
Before applying ANDROGEL 1.62% make sure that your shoulders and upper arms are clean, dry, and that there is no broken skin.
ANDROGEL 1.62% is to be applied to the area of your shoulders and upper arms that will be covered by a short sleeve t-shirt (See Figure A). Do not apply ANDROGEL 1.62% to any other parts of your body such as your stomach area (abdomen), penis, scrotum, chest, armpits (axillae), or knees.


(Figure A)

If you are using ANDROGEL 1.62% pump:

Before using a new bottle of ANDROGEL 1.62 % for the first time, you will need to remove the cap and then prime the pump. To prime the ANDROGEL 1.62% pump, slowly push the pump all the way down 3 times, over the sink drain. Do not use any ANDROGEL 1.62% that came out while priming. Wash it down the sink to avoid accidental exposure to others. Your ANDROGEL 1.62% pump is now ready to use.
Remove the cap from the pump. Then, put the spout opening at the top of the pump where the medicine comes out over the palm of your hand and slowly push the pump all the way down. Apply ANDROGEL 1.62% to the application site. You may also apply ANDROGEL 1.62% directly to the application site. Your healthcare provider will tell you the number of times to press the pump for each dose.
Wash your hands with soap and water right away.

Find Your Dose as Prescribed by Your Healthcare Provider		Application Method
1 pump	20.25 mg	Apply 1 pump of ANDROGEL 1.62% to 1 upper arm and shoulder.
2 pumps	40.5 mg	Apply 1 pump of ANDROGEL 1.62% to 1 upper arm and shoulder and then apply 1 pump of ANDROGEL 1.62% to the opposite upper arm and shoulder.
3 pumps	60.75 mg	Apply 2 pumps of ANDROGEL 1.62% to 1 upper arm and shoulder and then apply 1 pump of ANDROGEL 1.62% to the opposite upper arm and shoulder.
4 pumps	81 mg	Apply 2 pumps of ANDROGEL 1.62% to 1 upper arm and shoulder and then apply 2 pumps of ANDROGEL 1.62% to the opposite upper arm and shoulder.

If you are using ANDROGEL 1.62% packets:

Tear open the packet completely at the dotted line. Squeeze from the bottom of the packet to the top.
Squeeze all of the ANDROGEL 1.62% out of the packet into the palm of your hand.
Apply ANDROGEL 1.62% to the application site. You may also apply ANDROGEL 1.62% directly to the application site.
Let the application site dry completely before putting on a t-shirt.
ANDROGEL 1.62% is flammable until dry. Let ANDROGEL 1.62% dry before smoking or going near an open flame.
Avoid showering, swimming or bathing for at least 2 hours after you apply ANDROGEL 1.62%.
Wash your hands right away with soap and water after applying ANDROGEL 1.62%.

Find Your Dose as Prescribed by Your Healthcare Provider		Application Method
One 20.25 mg packet	20.25 mg	Apply 1 packet of ANDROGEL 1.62% to 1 upper arm and shoulder.
One 40.5 mg packet	40.5 mg	Apply half of the 40.5 mg packet of ANDROGEL 1.62% to 1 upper arm and shoulder and then apply the remaining packet contents to the opposite upper arm and shoulder.
One 40.5 mg packet and one 20.25 mg packet	60.75 mg	Apply one 40.5 mg packet of ANDROGEL 1.62% to 1 upper arm and shoulder and then apply one 20.25 mg packet of ANDROGEL 1.62% to the opposite upper arm and shoulder.
Two 40.5 mg packets	81 mg	Apply one 40.5 mg packet of ANDROGEL 1.62% to 1 upper arm and shoulder and then apply one 40.5 mg packet of ANDROGEL 1.62% to the opposite upper arm and shoulder.

How should I store ANDROGEL 1.62%?

Store ANDROGEL 1.62% at room temperature between 68ºF to 77ºF (20ºC to 25ºC).
When it is time to throw away the pump or packets, safely throw away used ANDROGEL 1.62% in the household trash. Be careful to prevent accidental exposure of children or pets.
Keep ANDROGEL 1.62% away from fire.

Keep ANDROGEL 1.62% and all medicines out of the reach of children.

This Instructions for Use has been approved by the U.S. Food and Drug Administration.

Revised: 11/2022