Belotero Lips Contour – 1 Siringa 0,6 ml

Belotero Lips Contour is indicated to correct atrophic scars of the face, for remodeling and contour of the lips and perioral fine wrinkles,

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Belotero Lips Contour it is a sterile, pyrogen-induced, viscoelastic, colorless and transparent Gel. It is an injectable and absorbable implant, indicated to correct atrophic scars of the face and for lip remodeling, lip contour, perioral fine wrinkles, moderate oral commissures. and’ composed of cross-linked sodium hyaluronate of non-animal origin and supplied in a saline phosphate buffer. Belotero Lips Contour contains 0.3% lidocaine hydrochloride. The presence of lidocaine is intended to reduce the pain locally associated with gel injection and to improve patient comfort.

Belotero Lips it is also available in version Shape.

Contains cross-linked sodium hyaluronate (22.5 mg/ml), lidocaine hydrochloride (3.0 mg/ml). Belotero Lips Contour should be used for injections into the superficial or middle dermis and the mucous membrane of the lips by a doctor duly qualified for this procedure. The doctor should keep in mind that the use of needles 30 G x 1/2 requires greater strength when injecting the gel than needles 27 G x 1/2. it must be injected slowly. The amount of gel to be injected depends on the area to be treated and the correction to be obtained. There is no need to correct. After injection, perform a light massage on the treated area, for even distribution of the product. For optimal use of Belostero Lips Contour, it is important that the needle is correctly inserted into the syringe. 1) Hold the glass cylinder of the syringe and the Luer-Lock adapter firmly between thumb and forefinger. 2) With your hand, hold the protective cap and unscrew it. 3) Push and rotate the needle on the syringe to the latch. Do not overtighten to prevent the Luer-Lock from moving and detaching from the syringe. 4) Continuing to hold the Luer-Lock, remove the needle sheath. Storage Store at a temperature between 2°C and 25°C. Protect from light and frost. Avoid mechanical shocks.

The package contains a pre-use disposable syringe – sterilized filled, 1 package leaflet, 2 traceability labels, 2 disposable sterile needles.

Size: 1 Syringe 0.6 ml

Do not inject into blood vessels, in areas that have skin problems of an inflammatory or infectious nature (acne, herpes, etc.) or in an area previously treated with permanent dermal filler. It is recommended to propose to these patients to undergo a double preliminary test and not to inject the product if the disease is progressing. It is also recommended to carefully monitor these patients after injection. It is recommended not to inject in patients with a history of streptococcal infections and in patients predisposed to hypertrophic or keloid scars. it must not be used in combination with other aesthetic medicine techniques such as delamination (peeling), dermoabrasion or any other type of laser treatment, before the complete healing of the last treatment. Keep in mind that even if healing is achieved earlier than expected, Belotero Lips Contour should not be used earlier than 2 weeks after the last treatment. Before use, check the integrity of the inner packaging and the expiration date of both the syringe and the needle. Do not use these products after the expiration date and if the package has been opened or damaged. Patients taking antithrombotic substances, such as aspirin or nonsteroidal anti-inflammatory drugs, are more likely to develop reactions such as hematomas, nodules or bleeding at the injection site. In the case of patients with epilepsy, impaired heart function, severe impairment of liver function or severe renal dysfunction or porphyria, the doctor should decide on a case-by-case basis whether to proceed with the injection of Belotero Lips Contour depending on the nature of the disease and the treatment in progress. Doctors and athletes must take into account the fact that lidocaine can cause positive results to anti tests – doping. Keep in mind that the presence of lidocaine can cause localized redness or hypersensitivity. Do not transfer to another container and do not add other ingredients to the product. After use, throw the syringe and the residual product. Do not resterilize and reuse, because of the risks associated with such practices, including infections. The patient should avoid makeup for at least 12 hours after treatment and should avoid saunas and steam rooms as well as prolonged exposure to the sun or UV rays for 2 weeks after treatment. Patients should also avoid exerting pressure and/or manipulating the treated area.

The application of the product is reserved exclusively for professional healthcare professionals with adequate qualifications. Therefore, we decline any responsibility for uses or applications of the product carried out by persons not qualified for health treatments.



Additional information

Weight0.3 kg


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