HEMANGEOL Physicians and Patients
A central library of patient education materials, physician resources, published data, and caregiver support organizations.
Physician Education Materials
Referral Form
Your healthcare provider can complete the referral form to enroll you in Eton Cares®, where you'll receive personalized support throughout your treatment journey.
Download Referral FormDerm Expert
Brochure report showcasing the three types of Infantile Hemangioma, the evolution of the disease, and the sequelae after involution of untreated hemangiomas.
Download The Derm Expert BrochurePrescribing Information
Full prescribing information, including indications and usage, dosage and administration, contraindications, warnings, and precautions.
Download Prescribing InformationPatient Education Materials
Patient Brochure
A caregiver brochure with information about HEMANGEOL and infantile hemangioma to share with families.
Instructions for Use
Parents and caregivers can follow these simple instructions to learn how to properly administer HEMANGEOL.
Getting Started Guide
Learn what to expect with your child’s HEMANGEOL prescription, including delivery, financial assistance, and ongoing support.
Medication Guide
Important safety information and usage guidance for parents and caregivers.
Physician Discussion Guide
A printable guide with key questions and talking points to help you have a productive conversation with your baby's physician.
Hemangioma FAQ (VBF)
Frequently asked questions about infantile hemangioma from the Vascular Birthmarks Foundation.
Caregiver Support and Patient Advocacy
When a baby first develops an infantile hemangioma, parents and caregivers may experience feelings of confusion, anxiousness, and guilt.
Below are organizations dedicated to providing education and support to all those affected by infantile hemangiomas.
The Vascular Birthmarks Foundation (VBF)
The Vascular Birthmarks Foundation is an international charitable organization that connects families affected by vascular birthmarks, tumors, or syndromes to the appropriate medical professionals. The foundation also provides informational resources, sponsors physician education, facilitates medical mission trips, and supports research and programs that promote acceptance for individuals with birthmarks.
The PHACE Syndrome Community (PSC)
PO Box 300
Willow Grove, PA 19090 USA
Phone: 1 (678) 744-3971
Email: info@phacesyndromecommunity.org
Website: phacesyndromecommunity.org
The PHACE Syndrome Community is a United States 501(c)(3) non-profit dedicated to serving those affected by PHACE syndrome along with their families, friends, and surrounding community. Its mission is to raise awareness of PHACE syndrome, build community for all affected, support research, and serve as a key source of medical information and the latest advancements.