Skin Booster Mandates

NCTF® 135 HA is a Class III medical device used for aesthetic skin revitalisation treatments. Treatment should only be performed by a qualified healthcare professional following consultation to determine suitability. As with all injectable treatments, there are potential risks and side effects

Inno-ce is below - other products mandatory statements can be found on the Intouch medical website 

INNO-CE® MOIST 1.5 is a class III medical device. A non-crosslinked hyaluronic acid solution (15mg/ml) designed to deliver immediate and long-lasting skin hydration by enhancing water retention and improving skin elasticity. Indicated for patients with dehydrated and revitalized skin requiring intensive hydration and improved skin barrier function. INNO-CE® MOIST 1.5 has risks and benefits. Refer to instructions for use.
Precautions and Contraindications:
Do not use in patients allergic to hyaluronic acid or any other component of the product.
Do not use in patients with active skin infections in the treatment area.
People with autoimmune diseases or under immunosuppressive treatment, in this case it would be a partial contraindication since it would depend on the patients condition.
Pregnant or breastfeeding women.
Certain diseases such as porphyria or hemorrhagic disorders, also a partial contraindication.

Ask your doctor if INNO-CE® MOIST 1.5 is right for you. For product information check with your doctor or product details with the Distributor, Intouch Medical Ltd, 171 Marua Rd, Mt Wellington, Auckland, NZ.
Exclusively for use by medical professionals trained in dermal injection techniques.

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 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

Anti-Wrinkle Mandates

MANDATORY INFORMATION / STATEMENT 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 www.medsafe.govt.nz . Click for further details Merz, Sydney. Distributed by Healthcare Logistics, Auckland  

Mantory Information | Statement Belotero® FULL CONSUMER MANDATORY INFORMATION / STATEMENT 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 Advertising Guidelines | JC Injectables Limited 5 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 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  

Dermal Filler Mandates

• 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.

• 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.