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 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.

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.

XEOMIN®

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.

RESTYLANE®

ASK YOUR HEALTH CARE PROFESSIONAL IF RESTYLANE® IS RIGHT FOR YOU.

RESTYLANE® is an unfunded medicine device. Product and treatment costs apply. Restylane®, Class III medical device, is a gel containing hyaluronic acid 20 mg/mL and lidocaine 0.3%, for injection by a healthcare professional into or below the skin to smooth facial wrinkles and enhance lips. Restylane® has risks and benefits. Ask your healthcare professional if Restylane® 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 precautions and contraindications, see www.galdermaaesthetics.com/nz. Restylane® is a registered trademarks of Galderma Holding S.A.

RESTYLANE® Skinbooster

ASK YOUR HEALTH CARE PROFESSIONAL IF RESTYLANE® SKINBOOSTER IS RIGHT FOR YOU.

RESTYLANE® Skinbooster is an unfunded medicine device. Product and treatment costs apply. Restylane® Skinboosters, Class III medical device, is a gel containing hyaluronic acid 20 mg/mL and lidocaine 0.3%, for injection by a healthcare professional into or below the skin to improve skin structure, hydration and elasticity. Restylane® Skinboosters has risks and benefits. Ask your healthcare professional if Restylane® Skinboosters 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 precautions and contraindications, see www.galdermaaesthetics.com/nz. Restylane® is a registered trademarks of Galderma Holding S.A.

SCULPTRA®

ASK YOUR HEALTH CARE PROFESSIONAL IF SCULPTRA® IS RIGHT FOR YOU.

SCULPTRA is an unfunded medicine device. Product and treatment costs apply. Sculptra®, Class III medical device, is a 150 mg poly-L-lactic acid implant liquid for injection by a healthcare professional into or below the skin to improve the volume of depressed areas such as in wrinkles and folds, skin aging and facial fat loss. Sculptra® has risks and benefits. Ask your healthcare professional if Sculptra® 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 precautions and contraindications, see www.galdermaaesthetics.com/nz. Sculptra® is a registered trademarks of Galderma Holding S.A.

JUVEDERM®

ASK YOUR HEALTH CARE PROFESSIONAL IF JUVEDERM® IS RIGHT FOR YOU.

JUVEDERM is an unfunded medicine device. Product and treatment costs apply. JUVÉDERM® a class III medical device must be administered by a healthcare professional. Always read and follow the instructions. The JUVÉDERM® range of products is a smooth, clear, colourless gel that contains hyaluronic acid to help correct or enhance facial contours; to define, correct or enhance lips; or improve the tone, texture and hydration of the skin. It also contains lidocaine (local anaesthetic) which helps improve comfort to the patient during injection. JUVÉDERM® has risks and benefits. For more information, please read the Patient Information Leaflets available on request from Allergan Aesthetics by phoning 0800 659 912 or from allerganaesthetics.com.au/products. JUVÉDERM® VOLBELLA® VOLIFT® VOLITE™ VOLUMA® and VOLUX™ are registered trademarks and trademarks of Allergan an Abbvie Company.

BELOTERO®

ASK YOUR HEALTH CARE PROFESSIONAL IF BELOTERO® IS RIGHT FOR YOU.

Belotero® is a Class III medical device to smooth facial wrinkles and folds, correct facial atrophic scars, restore of enhance the lips or restore facial volume. Belotero has risk and benefits. Ask your specialist if Belotero® is right for you. Contains transparent cross-linked sodium hyaluronate gel of nonanimal origin with lidocaine 0.3% to reduce local pain. Do not use if you have a skin inflammation or a skin infection or until the infection is healed. Precautions. There is a risk of infection. Tell your doctor if you are on blood-clotting medicines as there could be an increased risk of bruising or bleeding at the injection site. Possible side effects: swelling, bruising, redness hardening of the skin, pain, altered colour or itching. Lasts 6-12 months. You will need to pay for this product and doctor’s fees apply. Merz, Sydney. Distributed by Healthcare Logistics, Auckland.

BELOTERO® Revive

ASK YOUR HEALTH CARE PROFESSIONAL IF BELOTERO® REVIVE IS RIGHT FOR YOU.

BELOTERO® Revive is an injectable resorbable implant intended to revitalize facial skin through rehydration of dry and very dry skin, improvement of elasticity and firmness, and smoothening of superficial fine lines by reducing skin roughness. Belotero® Revive is indicated for revitalization of early-onset photodamaged facial skin, as characterized by dehydration, loss of elasticity and firmness, and presence of superficial fine lines. You should tell your practitioner and avoid treatment with BELOTERO® Revive if you: have had an allergic reaction to any of the ingredients; if you tend to develop keloids or heavy scars; have any bleeding disorders, poor wound healing, inflamed or infected skin, active auto-immune disease or general infection; are under the age of 18; are pregnant or breastfeeding. Please inform your practitioner of any diseases you have or have had. These include in particular cardiovascular diseases, autoimmune diseases, diabetes, epilepsy, liver or kidney problems, skin infections or severe allergies. If you take medication or vitamins, have had previous cosmetic procedures, or have been treated with other implants, please inform your practitioner. Always read the label and consult your Healthcare Professional for more information. This medical device must be administered by a Healthcare Professional. Copyright © 2023. Pharmacy Retailing NZ Limited t/a Health Care Logistics (HCL) 58 Richard Pearse Drive, Mangere, Auckland 2022. All rights reserved. Belotero® and Merz Aesthetics are registered trademarks of Merz Pharma GMbH & Co. KGaA.

RADIESSE®

ASK YOUR HEALTH CARE PROFESSIONAL IF RADIESSE® IS RIGHT FOR YOU.

Radiesse® injectable implant is intended for plastic and reconstructive surgery, including deep dermal and sub-dermal soft tissue augmentation of the facial area and dorsum of the hands. Radiesse® injectable implant is indicated for: the treatment of nasolabial folds, marionette lines or jawline; the augmentation of cheeks; the hand augmentation to correct volume loss in the dorsum of the hands; and the restoration and/or correction of the signs of facial fat loss (lipoatrophy) in people with human immunodeficiency virus. Radiesse® (+) Lidocaine injectable implant is intended for plastic and reconstructive surgery, including deep dermal and sub-dermal soft tissue augmentation of the facial area and dorsum of the hands in adults. Radiesse® (+) Lidocaine injectable implant is indicated for: the treatment of nasolabial folds, marionette lines and jawline; the augmentation of cheeks; hand augmentation to correct volume loss in the dorsum of the hands; the restoration and/or correction of the signs of fat or volume loss (lipoatrophy) in the facial area and for rejuvenation of the hands fat loss (lipoatrophy) in people with human immunodeficiency virus. You should tell your practitioner and avoid treatment with Radiesse®/Radiesse® (+) Lidocaine if you: have had an allergic reaction to any of the ingredients or have severe allergies including anaphylaxis; if you tend to develop keloids or heavy scars; have any bleeding disorders, poor wound healing; inflamed or infected skin; are under the age of 18; are pregnant or breastfeeding. Please inform your practitioner of any diseases you have or have had. These include in particular cardiovascular diseases, autoimmune diseases, diabetes, tumors, skin infections or severe allergies. If you take medication or vitamins, have had previous cosmetic procedures, or have been treated with other implants, please inform your practitioner. Always read the label and consult your Healthcare Professional for more information. This medical device must be administered by a Healthcare Professional. Merz Australia Pty Ltd (ACN: 151 073 559) Sydney, Australia. NZ Distribution: Pharmacy Retailing NZ Limited t/a Health Care Logistics (HCL). 58 Richard Pearse Drive, Mangere, Auckland 2022. For more information please phone 0800 822 310.

TEOSYAL®

TEOSYAL RHA® 1, TEOSYAL RHA® 2, TEOSYAL RHA® 3, TEOSYAL RHA® 4, TEOSYAL® PURESENSE REDENSITY 1, TEOSYAL® PURESENSE REDENSITY 2, TEOSYAL PURESENSE KISS®, TEOSYAL® PURESENSE GLOBAL ACTION, TEOSYAL® PURESENSE DEEP LINES, TEOSYAL® PURESENSE ULTIMATE and TEOSYAL® PURESENSE ULTRA DEEP TEOSYAL KISS®, RHA KISS®, TEOSYAL® MESO, TEOSYAL® GLOBAL ACTION, TEOSYAL® DEEP LINES, TEOSYAL® ULTIMATE and TEOSYAL® ULTRA DEEP are trademarks of the firm TEOXANE SA. These products are gel that contains hyaluronic acid, and 0.3% by weight of lidocaine hydrochloride. They are class III medical devices. Caution for people on blood thinning medicines. Local side effects: inflammatory reactions (redness, oedema, pain at the point of injection), haematomas, itching, temporary loss of sensitivity around the injected area, disorders of pigmentation in skin and hair, abscesses, indurations, nodules (possibly granulomas). General manifestations: immediate hypersensitivity up to anaphylactic shock, migration of the implant. Rare but serious adverse events associated with the intravascular injection of soft tissue fillers in the face have been reported and include temporary or permanent vision impairment or blindness, skin necrosis and stroke. Lasts 9-12 months. Please consult your doctor pharmacist for more information. Please refer to instructions for use, local distributor. Healthcare Logistics, Auckland.

Unbranded / i.e. antiwrinkle Injection or botulinum toxin injections

ASK YOUR HEALTH CARE PROFESSIONAL IF ANTI-WRINKLE INJECTIONS WITH BOTULINUM TOXIN IS RIGHT FOR YOU.

Botulinum toxin injections are prescription medicine for the treatment of frown lines , horizontal forehead lines and crow’s feet round the eyes. Botulinum toxin injections have risks and benefits. Ask your doctor if botulinum toxin injection is right for you. If you have side effects, see your doctor. You will need to pay for your botulinum toxin injection and clinic fees will apply. For details on precautions & side effects consult your doctor or go to www.medsafe.govt.nz . Botulinum toxin injections lasts about 4 months and further courses of treatment may be necessary. Should only be administered by trained medical professionals.