Consultations
Free in-person and video options before choosing a treatment.
30 minutes
Auckland Central cosmetic injectable clinic
Natural-looking cosmetic injectables tailored to your unique features and goals.
Treatment menu
Free in-person and video options before choosing a treatment.
30 minutesOne, two, and three area options available online.
30-45 minutesLips, cheeks, folds, marionette lines, and dissolving consults.
30 minutesProfhilo first treatment and Profhilo Body booking options.
30-45 minutesHow it works
Start with a conversation about goals, suitability, timing, and expectations.
Care takes place in a clean, professional setting with careful preparation and safety-focused treatment steps.
Results are tailored to your features, with a natural-looking finish as the guiding goal.
Review appointments are available through the booking portal when needed.
Combining clinical expertise with a focus on facial harmony and natural-looking rejuvenation.
Prices and availability may change. The booking portal is final for current pricing, deposits, and times.
Ready when you are
Book online securely, or call/text for flexible Sunday times by request.
Visit
Cosmetic injectable appointments require individual consultation and suitability assessment. Information on this website is general and does not replace personalised clinical advice.
Required product information
These statements are provided so medicine and device information can be read clearly before booking. Please ask Wei or your health care professional if any treatment is right for you.
ASK YOUR HEALTH CARE PROFESSIONAL IF BOTOX® IS RIGHT FOR YOU. BOTOX® is an unfunded medicine for aesthetic procedures so you will need to pay for the medicine and any other charges. BOTOX® is a Prescription Medicine containing 50, 100 or 200 units of clostridium botulinum Type A toxin complex for injection. It is used for the treatment of frown lines, crows feet and horizontal forehead lines. It should be administered only by trained medical professionals. Cautions: people with defective neuro-muscular transmission disorders, presence of infection at site of injection, glaucoma, pregnancy and lactation. Possible side effects include headaches, pain, burning or redness at injection site, local muscle weakness including drooping eye lids, lack of feeling & nausea. Talk to your specialist about the benefits/risks of this procedure or if you have concerns or side effects. For more information, please refer to the BOTOX® Consumer Medicine Information on the MEDSAFE website http://www.medsafe.govt.nz Note: BOTOX® treatment lasts about four months and after this time further courses of treatment may be necessary. Speak to your specialist about your own situation. BOTOX® and its design are trademarks of Allergan, Inc., an AbbVie company.
Juvederm Ultra™ & Juvederm Ultra Plus™ are medical devices Class III for the filling of medium size and deep facial wrinkles by injection into the skin and for creating definition and volume in the lips. Contains 24mg/mL. cross-linked hyaluronic acid. Juvederm has risks and benefits. Cautions: Use in an area that has been treated with another dermal filler, people with autoimmune disease, or who are pregnant, breastfeeding, under 18 years of age or have an increased susceptibility to keloid formation and hypertrophic scarring. People on blood thinning medicines. Possible side effects: injection site inflammatory reactions (redness/swelling, itching/pain on pressure) induration or nodules; discolouration; weak filling effect. If you have side effects or concerns speak to your doctor. Product and treatment costs will apply.
ASK YOUR HEALTH CARE PROFESSIONAL IF XEOMIN® IS RIGHT FOR YOU. XEOMIN® is an unfunded medicine for aesthetic procedures so you will need to pay for the medicine and any other charges. XEOMIN® (Incobotulinumtoxin A) 50, 100 Units is a Prescription Medicine. Indications: In adults, for the treatment of cervical dystonia; blepharospasm; spasticity of the upper limb; upper facial lines: glabellar frown lines, lateral periorbital lines (crow’s feet), horizontal forehead lines. XEOMIN® has both risks and benefits, consult your doctor if XEOMIN® is right for you. Further information on the risks and benefits of XEOMIN® can be found in the Consumer Medicine Information (CMI) available from www.medsafe.govt.nz or by calling 0800 822 310. Use strictly as directed. If symptoms continue or you have side effects, see your doctor, pharmacist or health care professional. Common side effects include: Headaches; nausea; tenderness, swelling, redness, numbness or bruising of the skin; dry eye; heavy feeling of eyelid/ eyebrow/forehead; face/brow not symmetrical, dropping eyelids/eyebrows. Serious side effects are rare and include allergic reactions. XEOMIN® and Merz Aesthetics are registered trademarks of Merz Pharma GmbH & Co. KGaA.
SKINVIVE by JUVÉDERM® is a medical device Class III used as an injectable implant for the treatment, by filling, of superficial cutaneous depressions such as fine lines and for additional improvement of skin quality attributes such as hydration and elasticity, via intradermal injection. Contains 12mg/mL. cross-linked hyaluronic acid with lidocaine hydrochloride monohydrate 3 mg/L. SKINVIVE by JUVÉDERM® has risks and benefits. This medical device must be administered by a healthcare professional. Cautions: Use in an area that has been treated with another dermal filler, people with autoimmune disease, history of severe and/or multiple allergies, or who are pregnant, breastfeeding, under 21 years of age or have an increased susceptibility to keloid formation and hypertrophic scarring, people on blood thinning medicines. Possible side effects: injection site inflammatory reactions (redness, lumps/bumps, swelling, bruising, pain, tenderness, firmness, discoloration and itching). Additionally, there have been reports of inflammation, nodules, unsatisfactory result, loss or lack of improvement, allergic reaction, anxiety, blood vessel blockage, infection, dry skin, increase or decrease in sensation, and abscess. If you have side effects or concerns speak to your doctor. Product and treatment costs will apply. For product information check with your doctor or product information at Allergan (NZ) Limited, Auckland.
ASK YOUR HEALTH CARE PROFESSIONAL IF PROFHILO® IS RIGHT FOR YOU. PROFHILO® and PROFHILO® Body is an unfunded medicine so you will need to pay for the medicine and any other charges. PROFHILO® and PROFHILO® Body are Class III medical devices containing 16mg high molecular weight (MW) hyaluronic acid (HA) + 16mg low MW HA/1mL syringe that is obtained through a patented treatment (NAHYCO® Hybrid Technology) which provides it with unique characteristics for its use in the face and body, where it is injected with an ultrafine needle to plump the skin to smooth away wrinkles and improve texture and skin quality. PROFHILO® must only be administered by a medical practitioner or a qualified nurse injector (who operates under the supervision of a medical practitioner). Treatment costs and normal practitioner's fees will apply. PROFHILO® has risks and benefits. Do not use with treatments such a laser resurfacing or medium deep skin-peeling. Do not inject into inflamed areas or intravenously or intramuscularly. Please consult your medical practitioner regarding its suitability for you, or if there are any questions regarding precautions and side effects. For further product information, please refer to your medical practitioner or the Instructions for Use leaflet at Dermocosmètica PTY LTD, Australia. PROFHILO® is a registered trademark of IBSA.
ASK YOUR HEALTH CARE PROFESSIONAL IF SUNEKOS® IS RIGHT FOR YOU. SUNEKOS® is an unfunded medicine so you will need to pay for the medicine and any other charges. SUNEKOS® is a Class III medical devices containing a patented formula of HA and amino acids. SUNEKOS® is a resorbable injection solution that modifies the structure of mature skin, restoring volume, filling wrinkles and folds in the skin and in scar sites. SUNEKOS® has risks and benefits. SUNEKOS® should not be used on patients: with known hypersensitivity to any of its components; presenting with a general infection, inflammation or irritation in the area to be treated; or in patients predisposed to coagulation disorders. A local reaction may rarely occur, caused by hypersensitization phenomena, with symptoms that include oedema and sensation of burning and/or itching. These reactions normally resolve within two days. Consult your healthcare professional to see if SUNEKOS® is right for you. For more information refer to the instructions for use. New Zealand Sponsor: AA-Med Pty Ltd Distributed by: Xytide Biotech NZ Pty LTD.