Injectable Program · PDO product identity · Bangkok
Ultracol
Program
A consultation-led page for people comparing injectable options.
The exact product variant, treatment area, amount, session plan, risks, alternatives and current itemised quotation must be confirmed before treatment.
- Appointment
- Varies by area and individual
- Recovery
- Daily activity is often possible; response varies
- Comfort
- Discomfort varies by area and skin condition
- Material
- PDO microspheres; verify the exact variant
Overview
What is Ultracol Program?
Ultracol Program is a medical-device product based on biodegradable PDO (polydioxanone) microspheres.
The manufacturer's current public information describes a Korea MFDS-approved indication for temporary improvement of bilateral nasolabial folds.
The exact product variant, planned area, amount and local product documentation used at Waleerat Clinic must be verified during consultation.
Ultracol Program is not PDRN, salmon-derived material or an HA filler.
General information only. It is not a diagnosis or a recommendation for treatment. Suitability and response vary.
Open official service sourceThe questions that change this decision.
Focus on the outcome, timing, material or trade-offs that matter for this Program.
Is Ultracol Program PDRN or made from salmon?
No.
The current manufacturer information identifies the product material as PDO (polydioxanone) microspheres.
Ask the clinic to show the exact variant and local product documentation because similar-sounding injectable names are not interchangeable.
What is the difference between Ultracol Program 100 and Ultracol Program 200?
The currently verified public manufacturer page does not provide a complete side-by-side instructions-for-use comparison.
Do not infer that the variants are interchangeable from a product name or online image.
Confirm the sealed variant, local label, intended area, amount and current instructions for use before deciding.
How many Ultracol Program sessions are needed?
A 2024 study of 31 adults with nasolabial folds used two ULTRACOL100 applications four weeks apart.
That small, short study protocol is not a universal schedule for every variant, area or person.
The session plan should follow assessment, the exact product documentation and review of response.
When are changes assessed and how long do they last?
The 2024 ULTRACOL100 study assessed participants four weeks after each application and followed the two-session protocol for eight weeks.
It therefore does not establish a universal long-term duration.
Agree on a review point and avoid treating an old promotional duration as a guarantee.
Is Ultracol Program established for the under-eye area?
The manufacturer’s current public English page states a Korea MFDS-approved indication for temporary improvement of bilateral nasolabial folds.
The verified source set used for this page does not establish an under-eye indication.
Under-eye concerns, previous procedures and alternatives need a separate physician assessment.
What do the current safety data show?
In the 31-person ULTRACOL100 study, no participant withdrew early because of a treatment-related adverse effect during the short follow-up.
The authors also identified the small sample and short follow-up as limitations and called for larger and longer safety evaluation.
This is not proof that uncommon or long-term complications cannot occur.
What should I disclose before comparing Ultracol Program with filler or another injectable?
Share prior procedures in the area, medicines and supplements, allergies, health conditions, pregnancy or breastfeeding, future surgery plans and any important travel or event date.
The verified evidence does not support one universal sequence with filler or other injectables; the comparison must be individualized.
How is the Ultracol Program price compared with alternatives?
Use a current itemised quotation that names the exact product and variant, vial or quantity basis, area, physician fee, comfort plan, aftercare and follow-up.
A headline price cannot be compared fairly when the product, amount or plan differs.
Before deciding
The service-specific limit to confirm.
The point below is specific to this Program. Your own assessment and written instructions take priority.
Verify the sealed product, exact variant, lot, expiry, local label and instructions for use before treatment.
Do not rely on an online photograph to confirm authenticity, and do not use legacy PDRN or salmon-derived descriptions for Ultracol Program.
Questions before you choose.
Can international visitors consult before travelling?
Yes.
Share your preferred language and travel dates through an international contact channel.
Confirm appointment timing, material requirements and follow-up arrangements before travelling.
Choose how to reach us.
Use the channel that works best for appointment coordination and general questions.
Messaging is not monitored as an emergency service. Language availability and response times can vary.