Skin x ZIIP Lift & Brighten Kit

CurrentBody Skin LED Light Therapy Face Mask:

Before carrying out your first treatment you must carry out a sensitivity test. Follow the step by step guide below;

1. Power on your device.

2. Switch ON the controller and allow the device to run for its full 10-minute treatment program. The device will automatically switch off after 10 minutes.

3. At any time if your skin feels HOT or uncomfortable STOP using the device immediately.

4. After the treatment, wait at least 6 hours. If the skin appears red and/or itchy the device is unsuitable for you.

5. Return the device to CurrentBody within 14 days for a full refund.

ZIIP HALO:

Prior to use, make sure your skin is dry, clean and free from skincare products such as moisturisers, serums or makeup. Make sure you remove all jewellery from the treatment area and from your hands. If you have used an oil cleanser, please ensure there is none left on the skin. Oil will stop the ZIIP HALO from working. Those with facial hair should shave before use. Hair can interfere with the conductivity of the globes and the device will not work.

Apply a thumbnail size amount of Electric Complex Gel to the treatment area and spread it evenly to the size of the palm of your hand.

Switch on your ZIIP HALO and move in small circular motions over the gel for 3 minutes.

Stop the test immediately if you do not feel comfortable or if you see adverse effects.

Wait 48 hours and examine the tested area. If the skin in the tested area appears normal you can start a full treatment.

CurrentBody Skin LED Light Therapy Mask:

DO NOT use this device to treat any other conditions apart from those listed in the indications for use. This device has not been tested for any other conditions than those listed, and the risk is unknown.

DO NOT use this device if you are pregnant, planning on becoming pregnant or breastfeeding. This device has NOT been tested on pregnant or breast-feeding women and therefore the risk to the foetus, neonate or pregnant women is unknown.

DO NOT use this device if you suffer from Lupus erythematosus, photosensitive eczema or Albinism. If you use this device system to treat Lupus erythematosus, photosensitive eczema or Albinism you may cause a severe skin reaction.

DO NOT use this device if you suffer from any photosensitive disorder (sensitisation to light). If you use this device and you suffer from a photosensitive disorder you may cause a severe skin reaction.

DO NOT use the device if you suffer from light-induced headaches.

DO NOT use the device if you suffer from any genetic conditions of the eye.

DO NOT use this device if you are taking any medication that can cause photosensitivity. If you use this device and you are taking any medication that can cause photosensitivity you may cause a severe skin reaction. Photosensitivity is a common side effect of various medications. These can include certain antibiotics, chemotherapy drugs, and diuretics. If you are unsure about any medication you may be taking consult your healthcare provider. Other substances not listed above can also cause photosensitivity. Common examples of these substances are St John's Wort, Coal tar, deodorants, antibacterial soaps, artificial sweeteners, naphthalene (moth balls), petroleum products, brightening agents found in laundry detergent, and cadmium sulphide (a chemical injected into the skin during tattooing.

ZIIP HALO:

ZIIP HALO should NOT be used by people who are under the age of 18 years, are pregnant, are subject to seizures, including suspected or diagnosed epilepsy, have cancer/tumours, have a cardiac pacemaker with implanted defibrillators/ stimulators or have electronic implanted devices.

The device should NOT be used on or near cancerous lesions, or applied over swollen, infected or inflamed skin e.g., phlebitis, thrombophlebitis, broken capillaries, varicose veins etc.

DO NOT apply stimulation across your chest as the introduction of electrical current into the chest may cause rhythm disturbances to your heart, which could be lethal.

DO NOT use this device on patients who have a cardiac pacemaker, implanted defibrillator, or other implanted metallic or electronic device, because this may cause electric shock.