Support for Picato® patients every step of the way


Picato® is now covered on more health insurance plans1
  • 8 out of 10 patients who are prescribed Picato® for their AK are covered with unrestricted coverage by commercial plans1
  • Picato® has preferred formulary status in 53% of cases when it is prescribed for AK in commercially insured patients1
LEO® Co-pay Savings Card

LEO® Co-pay Savings Card

Eligible* patients may pay as little as $35 by using the LEO® Co-pay Savings Card for Picato®, up to a $250 maximum benefit. For patients with commercial health insurance, this may reduce out-of-pocket expenses.

For more information, click here.


Your patients may be eligible* for automatic savings with the eVoucherRx Program. To search for participating pharmacy locations, have your patients visit
. If they fill their prescription at any nonparticipating pharmacy, your patients may present their LEO® Co-pay Savings Card to their pharmacist along with an eligible prescription to receive a co-pay discount.

*Certain restrictions apply. For patients with commercial health insurance, this card may reduce out-of-pocket expenses.
Must be 18 years of age or older to be eligible. For eligibility requirements and program restrictions, visit or
call 1-855-242-6936.

Indications and Usage

Picato® (ingenol mebutate) gel, 0.015%, 0.05% is indicated for the topical treatment of actinic keratosis.

Important Safety Information

Picato® is contraindicated in patients with known hypersensitivity to ingenol mebutate or any component of the formulation. Anaphylaxis, as well as allergic reactions leading to hospitalization have been reported in postmarketing use with Picato®. If anaphylactic or other clinically significant hypersensitivity reactions occur, discontinue Picato® immediately and institute appropriate medical therapy.

For topical use only; not for oral, ophthalmic, or intravaginal use. Avoid treatment in, near, or around the periocular area, mouth and lips. Inform patients that hypersensitivity reactions and/or ophthalmic adverse reactions can occur with Picato®. Eye disorders, including severe eye pain, chemical conjunctivitis, corneal burn, eyelid edema, eyelid ptosis, periorbital edema can occur after exposure. To avoid transfer of the drug into the eyes and to the periocular area during and after application, patients should wash hands well after applying Picato® gel. If accidental exposure occurs, flush eyes with water and seek medical care.

In post-approval use of Picato®, the following adverse reactions have been identified: hypersensitivity (including anaphylaxis), allergic contact dermatitis, application site pigmentation changes, application site scarring and herpes zoster. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

Severe skin reactions in the treated areas on the face/scalp and trunk/extremities, including erythema, flaking/scaling, crusting, swelling, vesiculation/pustulation, and erosion/ulceration can occur after application. Administration of Picato® gel is not recommended until the skin is healed from any previous drug or surgical treatment. The most common adverse reactions observed in clinical trials on the face and scalp (≥2%) are local skin reactions (94%), application site pain (15%), application site pruritus (8%), application site infection (3%), periorbital edema (3%), and headache (2%). The most common adverse reactions observed in clinical trials on the trunk and extremities (≥2%) are local skin reactions (92%), application site pruritus (8%), application site irritation (4%), nasopharyngitis (2%), and application site pain (2%).

There are no adequate and well-controlled studies of Picato® gel in pregnant women. Picato® gel should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

The safety and effectiveness of Picato® gel for actinic keratosis in patients under 18 years of age has not been established.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit or call 1-800-FDA-1088.

This site is intended for US residents only. The products discussed on this site may have different product labeling in different countries.

Click here for Full Prescribing Information.