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

BOTOX® is an unfunded Prescription Medicine for aesthetic procedures so you will need to pay for the medicine and any other charges. BOTOX® containing 50,100 or 200 units of clostridium botulinum Type A toxin complex for injection. It is used for the aesthetic treatment of frown lines, crow’s 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. BOTOX® and its design are trademarks of Allergan, Inc., an AbbVie company. Aesthetic clinic name and city/town location

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

Dysport® is an unfunded Prescription Medicine for aesthetic indications, product and treatment costs apply. Dysport® 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 instruction 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. Aesthetic clinic name and city/town location

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

PROFHILO® family of products are unfunded medical devices product and treatment costs apply. PROFHILO® family of products are Class III medical devices containing 16mg high molecular weight (MW) hyaluronic acid (HA) + 16mg low MW HA/1mL syringe 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). PROFHILO® has risks and benefits. Talk to your healthcare professional about the benefits/risks of this procedure or if you have concerns or side effects. Always follow the instructions you are given. 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. Aesthetic clinic name and city/town location

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

BELKYRA® is an unfunded prescription medicine so you will need to pay for the medicine and any other charges. BELKYRA® Solution for injection contains deoxycholic acid (10 mg/mL) as the active ingredient. BELKYRA® injection non-surgically reduces fat under the chin, resulting in a more contoured neck profile and jawline. 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 BELKYRA® Consumer Medicine Information on the MEDSAFE website http://www.medsafe.govt.nz BELKYRA® is a trademark of Allergan Inc, an AbbVie company. Aesthetic clinic name and city/town location

Sunekos 1200 is an implantable medical device that modifies the structure of mature skin, restoring volume, filling wrinkles and folds in the skin and in scar sites. It is suitable for creating a temporary increase in the volume of skin tissue. Sunekos 1200 is a medical device that is sterile, injectable, non pyrogenic, biocompatible, re- absorbable, made with hyaluronic acid and amino acids.

Sunekos Performa is a medical device recommended for the treatment of blemishes and depressions in the skin caused by wrinkles and scars. Sunekos Performa is a sterile resorbable injectable solution which acts as a filler, supporting the restoration of physiological elasticity and temporarily replacing volume by expanding the soft tissues.

Sunekos should not be used on patients: with known hypersensitivity to any of its components; presenting with a general infection, inflammatory or infectious cutaneous problems; with history of severe multiple allergies or anaphylactic shock; prone to hypertrophic scars/keloids or streptococcal diseases; in patients presenting with porphyria; under 18 years of age; in pregnancy or lactation; others. See full
Instructions for use before prescribing for full safety information, available from www.xytide.co.nz

Copyright© 2024. Xytide Biotech Pty Ltd. Always read the label and follow the instructions. This medical device must be administered by a Healthcare Professional.

New Zealand Sponsor: AA-Med Pty Ltd

Distributed by: Xytide Biotech NZ Pty Ltd (NZBN 9429049668612) C/O Alliott Ltd, Level 2, 142 Broadway, Newmarket, Auckland 1023 NZ. For more information please phone +61 1800 570 036