Prescription-Only Treatment Information
At Luminous Skin, your safety and care are our top priority.
The following information is provided to meet advertising standards and ensure transparency around prescription-only cosmetic treatments available through consultation.
Mandatory Statement for Xeomin®
Xeomin® (incobotulinum toxin ) Prescription Medicine, for the treatment of upper facial lines: glabellar frown lines, crow’s feet round the eyes, horizontal forehead lines. Xeomin has risks and benefits. Ask your doctor if Xeomin is right for you. (incobotulinum toxin A, purified Botulinum toxin type A 50 Units and 100 Units . For product information check with your doctor or Consumer Medicine Information on medsafe for further details. Merz, Sydney. Distributed by Healthcare Logistics, Auckland.
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Mandatory Statement for PROFHILO®
PROFHILO® containing low & high molecular weight hyaluronic acid, is a Class III medical device for the treatment of the face and body for contours redefinition and laxity remodelling where skin laxity is a problem. Profhilo® has risks and benefits. Do not use with treatments such a laser resurfacing or medium deep skin-peeling. Caution in people on blood thinning medicines. Do not inject into inflamed areas or intravenously or intramuscularly. Possible side effects: pain and swelling at injection site. Accelagen Pty. Ltd. Whanganui.
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Mandatory Statement for PROFHILO® STRUCTURA
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
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Mandatory Statement for VISCODERM® HYDROBOOSTER
VISCODERM® HYDROBOOSTER is a Class III medical device containing 25mg/1mL of cross-linked hyaluronic acid, it is used to restore intradermal hydration and to keep improve the structure and elasticity of the skin. VISCODERM® HYDROBOOSTER 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. VISCODERM® HYDROBOOSTER has risks and benefits. If you have side effects or concerns, speak to your medical practitioner. Please consult your medical practitioner regarding its suitability for you. For further product information, please refer to your medical practitioner or the Instructions for Use leaflet at Dermocosmética PTY LTD, Australia.
Made in Italy. VISCODERM® HYDROBOOSTER is a registered trademark of IBSA. IBSA Farmaceutici S.r.l Via Martiri di Cefalonia 2 26900 Lodi – Italy. Distributed in New Zealand by Dermocosmética (NZBN 9429050049066) Suite A, Floor 8 Harbourview Building, 152 Quay St, Auckland Central, Auckland, New Zealand, through Healthcare Logistics. 58 Richard Pearse Drive, Airport Oaks, Manukau City, Auckland, New Zealand.
Copyright © Dermocosmetica 2024. All rights reserved. No part of this publication may be stored in a retrieval system or reproduced by any means whatsoever without written consent of the publisher.
To learn more about VISCODERM® HYDROBOOSTER go to www.ibsaderma.co.nz
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Mandatory Statement for Belotero®
Belotero® is a Class III medical device for the correction of facial wrinkles and folds, and for volume augmentation. Belotero® is an injectable medical device containing cross-linked sodium hyaluronate. Always read the label and consult your healthcare professional to see if this product is right for you. This medical device must be administered by a trained professional. Individual results may vary.
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