Mandatory Statements
BOTOX®
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
DYSPORT®
ASK YOUR HEALTH CARE PROFESSIONAL IF DYSPORT® IS RIGHT FOR YOU. Dysport® is an unfunded medicine for aesthetic indications. Product and treatment costs apply. Dysport® is a prescription medicine contains 300 or 500 U of botulinum toxin, distributed in NZ by Galderma Australia Pty Ltd, North Sydney, NSW, for the treatment of frown lines and crow’s feet around the eyes. Dysport® has risks and
benefits. Ask your healthcare professional if Dysport® is right for you and to explain the possible side effects. Tell them if any side effects concern you. ALWAYS FOLLOW THE INSTRUCTIONS YOU ARE GIVEN. For details on precautions and side effects, see the Consumer Medicines Information at www.medsafe.govt.nz. Dysport® is a registered trademark of Ipsen Pty Ltd. Galderma is a registered trademark of Galderma Holding S.A
RELFYDESS®
ASK YOUR HEALTH CARE PROFESSIONAL IF RELFYDESS® IS RIGHT FOR YOU. Relfydess is an unfunded medicine for aesthetic indications. Product and treatment costs apply. Relydess is a prescription medicine contains 150 units of relabetulinumtoxinA for the treatment of frown lines and crow’s feet around the eyes. Relfydess has risks and benefits. Ask your healthcare professional if Relfydess is right for you and to explain the possible side effects. Tell them if any side effects concern you. ALWAYS FOLLOW THE INSTRUCTIONS YOU ARE GIVEN. For details on precautions and side effects, see the Consumer Medicines Information at www.medsafe.govt.nz. Galderma Australia Pty Ltd. Galderma is a registered trademark of the Galderma Holding S.A. Distributed in New Zealand by Healthcare Logistics.
PROFHILO®
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. PROFHILO® STRUCTURA containing low and high molecular weight Hyaluronic acid is a class 3 medical device for face treatment and for restoring adipose tissues -in the dermal tissue repair process, and in
cases of acne scars.
PROFHILO® STRUCTURA has risks and benefits. Do not use it along with treatments such as laser resurfacing or medium/deep skin peeling. Do not inject into inflamed areas or intravenously or intramuscularly. Possible side effects are pain, itching or swelling at the injection site. Dermocosmetica Pty Ltd. Auckland. TAPS BG4145.
SUNEKOS®
ASK YOUR HEALTHCARE PROFESSIONAL IF SUNEKOS® IS RIGHT FOR YOU. Sunekos containing hyaluronic acid and amino acids is a class III medical device 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 hypersensitisation 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 LtdDistributed by:Xytide Biotech NZ Pty LTD
TEOXANE/TEOSYAL® DERMAL FILLERS
ASK YOUR HEALTH CARE PROFESSIONAL IF TEOXANE/TEOSYAL® IS RIGHT FOR YOU. Teoxane (Teosyal®) dermal fillers are Class III medical devices designed to restore facial volume, enhance contours, and soften wrinkles. Dermal filler treatments have risks and benefits. Ask your healthcare professional if these treatments are appropriate for you. These products contain hyaluronic acid, and some formulations include 0.3% lidocaine for client comfort. For more information, visit www.medsafe.govt.nz or consult your doctor. New Zealand Distributor: Healthcare Logistics, Auckland.
SKINPEN®
ASK YOUR HEALTH CARE PROFESSIONAL IF SKINPEN® IS RIGHT FOR YOU. The SkinPen® Precision system is a microneedling device and accessories intended to be used as a treatment to improve the appearance of wrinkles of the neck for Fitzpatrick skin types II – IV and to improve the appearance of facial acne scars in adults with all Fitzpatrick skin types aged 22 years and older. Indications and body treatment areas for SkinPen® Precision may vary based on your country. For more information, please visit www.skinpen.com/international. See intended use, important safety information, and FDA clinical trial data details at skinpen.com/international. Data on file. Crown Aesthetics. 2022