Important Product information

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.

 

DYSPORT®

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

Dysport® prescription medicine contains 300 or 500U of botulinum toxin, distributed in NZ by Healthcare Logistics, for the treatment of frown lines and crow’s feet around the eyes. Dysport® lasts up to 6 months and further courses of treatment may be necessary. It should only be administered by trained medical professionals. 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 or consult your healthcare professional. Unfunded for aesthetic indications. Product and treatment costs apply. Galderma Australia Pty Ltd, 58 Richard Pearse Drive, Airport Oaks, Mangere Auckland 2022. Distributed in NZ by Healthcare Logistics, 58 Richard Pearse Drive, Airport Oaks, Mangere Auckland 2022.

 

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 othercharges. 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 neuromuscular 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.

 

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 non-animal 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 bloodclotting 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

 

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. Accelagen Pty. Ltd. Whanganui.

 

PROFHILO® STRUCTURA

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

PROFHILO® STRUCTURA is a class III medical device and must be injected by a medical practitioner or a qualified nurse injector (operating under the supervision of a medical practitioner).PROFHILO® STRUCTURA [4.5% – 22.5 mg (H-HA) + 22.5 mg (L-HA)/1 ml Hyaluronic acid sodium salt and 4.5% – 45 mg (H-HA) + 45 mg (L-HA)/2 ml Hyaluronic acid sodium salt], injection gel in a single use sterile prefilled syringe. It is indicated for adults of both sexes for corrective / filling action of natural or induced skin depressions. PROFHILO® STRUCTURA has risks and benefits. Ask your healthcare professional if PROFHILO® STRUCTURA is right for you and to explain the possible side effects. WARNINGS & PRECAUTIONS: Do not use PROFHILO® STRUCTURA in case of known hypersensitivity or allergies to the components of the product. Do not use it in pregnant or breast-feeding women, in patients with autoimmune diseases. Do not inject intravascularly, into the muscles or tendons, or for breast enlargement. CONTRAINDICATIONS: PROFHILO® STRUCTURA must not be used in conjunction with treatments such as laser resurfacing and medium-deep peeling. Tell your doctor if any side effects concern you. ALWAYS FOLLOW THE INSTRUCTIONS YOU ARE GIVEN. Treatment costs and normal practitioner fees will apply. Please contact us for any further information or for the IFU (Instructions for use) of this product or for medical information or reporting any adverse effects. Distributed in New Zealand by Dermocosmètica (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.

 

SUNEKOS®

ASK YOUR HEALTH CARE 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, folds and scars.
Sunekos has risks and benefits. Treatment costs and normal practitioner fees will apply. 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 Ltd Distributed by: Xytide Biotech NZ Pty LTD, Auckland.

 

REJURAN

ASK YOUR HEALTH CARE PROFESSIONAL IF REJURAN IS RIGHT FOR YOU

Rejuan is a dermal tissue reconstructive injectable gel, derived from animal-based material. It is designed specifically for injection into the mid-to-deep dermal layer to
stimulate tissue repair and reconstruction, improving overall skin appearance. It works by activating the skin’s own regenerative ability to restore its own collagen structure and increase skin elasticity. Rejuran is a Class III Medical Device.Important notes: Must only administered by trained medical professionals. Treatment costs and normal practitioner fees will apply. Always discuss your individual situation with your healthcare professional to understand the full benefits and risks involved.PharmaResearch Co., Ltd. (South Korea). NZ Distributor: K Bridge Medical Pty Ltd Australia.

 

DermaPen

ASK YOUR HEALTH CARE PROFESSIONAL IF DERMAPEN IS RIGHT FOR YOU

DermaPen device and cartridge are Class IIa medical devices for electronic cosmetic micro-needling. To stimulate tissue regeneration and improve the appearance of the skin (to treat acne scarring, fine lines, wrinkles and patchy or irregular skin discolouration). All medicines, medical devices and treatments carry benefits and risks. Individual results may vary. Speak to your qualified Medical Skin Therapist to see what might be right for you and to explain the possible side effects. Always follow any instructions provided in terms of treatment aftercare. EquipmedTM (established 1976 in Australia). NZ Distributor: Probeauty, Auckland is the distributor for Dermapen in New Zealand.