Merz

Radiesse 1,5 cc, it is a unique filler in its kind approved in the United States by F. D. A. (Food and Drug Administration, the Agency for food and medicines) for the correction of facial folds and moderate and severe wrinkles, including nasolabial folds.In Europe, the radiese is CE certified for plastic and reconstructive surgery, including the increase in the soft intradermal and subcutaneous fabric of the facial area.

Radiesse 1.5 cc is indicated the treatment of periorbital wrinkles, cheeks, nasolabial folds, oral commissures, puppet lines, skin lip increase, volume increase in nose area, chin fold, lip contour (vermilion), chicken legs, lobes of'ear, malar region, jaw line and maxillary furrow and for the rejuvenation of the hand.

The 1.5cc Radiesse Filler is also available in Version with lidocaine.

Radiesse 1.5cc is a fillers composed of 30% from synthetic microspheres of Chaha hydroxiapitis of calcium suspended in watery solution of gel (70%).Calcium hydroxyapatitis microspheres have a size between 25 and 45 microns and are composed of calcium and phosphate ions that are also found in the epidermal fabric.It is a 100% biocompatible product and therefore no allergological tests are necessary before undergoing treatment.The action of the product is immediate and has a function of stimulus of natural collagen.During the injection, the gel in which Caha's microspheres are immersed an immediate corrective and filler action.

After the injection, Radiese 1.5cc has an action of stimulus to the production of natural collagen.The macrophages degrade the gelatinous medium that disappears in a few months and the fibroblasts form new natural collagen which will give a greater volume and smoother skin.For the specific characteristics of the product, a lower use of material is needed compared to a treatment with hyaluronic acid and therefore it is reached by a saving of 25-30% for each treatment, obtaining a more lasting effect than other fillers.The product is not permanent but completely biodegradable by the human body, so Radiesse is gradually metabolized by macrophages with the phagocytosis mechanism and totally eliminated by the body.Thanks to the longer duration, the effect, the duration of Radiesse is about a year, and in some cases longer periods of duration have been described. 

The application of the product is reserved exclusively for professional health workers with adequate qualification.Therefore, any liability for uses or applications of the product made by subjects not qualified for health treatments is declined.

1.5cc Radiesse with lidocaine, is a unique filler of its kind produced by Merz and approved in the United States by the F.D.A.(Food and Drug Administration, the food agency and medicines) for the correction of facial folds and moderate and severe wrinkles, including nasolabial folds.In Europe, 1.5 cc radiese, is CE certified for plastic and reconstructive surgery, including the increase in the soft intradermal and subcutaneous fabric of the facial area.The procedure is simple, comfortable e painless, as The product contains lidocaine, an anesthetic, in the quantity of 2%.

Radiesse 1.5 cc with lidocaine is indicated for the treatment of peri-orbital wrinkles, cheeks, nose-labial folds, oral commissures, puppet lines, skin labial increase, increase in volume nose area, fold of the chin, lip contour (vermilion), chicken legs, ear lobe, the malar region, mandibola line and maxillary furrow eper rejuvenation of the hand.

The 1.5cc Radiesse Filler is also available in Version without lidocaine.

Radiesse 1.5cc with lidocaine is a fillers composed of 30% from synthetic microspheres of Chaha hydroxiapitis of calcium suspended in watery solution of gel (70%).Calcium hydroxyapatitis microspheres have a size between 25 and 45 microns and are composed of calcium and phosphate ions that are also found in the epidermal fabric.It is a 100% biocompatible product and therefore no allergological tests are necessary before undergoing treatment.The action of the product is immediate and has a function of stimulus of natural collagen.During the injection, the gel in which Caha's microspheres are immersed an immediate corrective and filler action.

After the injection, 1.5cc radiese with lidocaine has an action of stimulus to the production of natural collagen.The macrophages degrade the gelatinous medium that disappears in a few months and the fibroblasts form new natural collagen which will give a greater volume and smoother skin.For the specific characteristics of the product, a lower use of material is needed compared to a treatment with hyaluronic acid and therefore it is reached by a saving of 25-30% for each treatment, obtaining a more lasting effect than other fillers.The product is not permanent but completely biodegradable by the human body, so Radiesse is gradually metabolized by macrophages with the phagocytosis mechanism and totally eliminated by the body.Thanks to the longer duration, the effect, the duration of Radiesse is about a year, and in some cases longer periods of duration have been described. 

The application of the product is reserved exclusively for professional health workers with adequate qualification.Therefore, any liability for uses or applications of the product made by subjects not qualified for health treatments is declined.

New Beloterian intense with lidocaine It is produced by Merz, it is supplied in disposable glass syringe, and is indicated to significantly correct or decrease deep skin depressions and to increase the volume in the presence of face volumetric defects.

New Beloterian intense with lidocaine is also available in Version without lidocaine And it allows you to correct facial depressions due to trauma or scars, deep wrinkles, furrows and to remodel the contours of the face by means of injections in areas of the face such as cheekbones, chin, etc.It also allows you to increase the volume of the lips, especially of the free margin and vermilion and contains lidocaine for better patient comfort during treatment.

Format: 1 Syringing reimbasped to 1 ml.

New Beloterian intense with lidocaine It is destined to be injected into the deep dermis by a legally enabled doctor.Because the treatment is successful, the doctor must have previously been trained in injection techniques aimed at increasing the volume of skin tissues.It is also essential to operate in adequate aseptic conditions.It should be injected into a healthy and not inflamed skin, disinfected.It is an isotonic, sterile, apoish, viscoelastic, clear, colorless and transparent gel.Not recommended in the event of a noteworthy hypersensitivity to any component of the product, especially to sodium hyaluronate, in the event of autoimmune or diabetes diseases, in the event of streptococcal diseases (for example, recurrent sore throat), in patients prepared for the keloids,In pregnant or breastfeeding women, in people who are less than 18 years old.Components: reticulated sodium hyaluronate: 25, 5 mg/ml;phosphate buffer pH 7 q.s.: 1, 0 ml;lidocaine.
 
The application of the product is reserved exclusively for professional health workers with adequate qualification.Therefore, any liability for uses or applications of the product made by subjects not qualified for health treatments is declined.

Belotero SOFT It contains 20 mg/ml of has linked cross, is indicated to increase the volume of the skin tissue and allows you to correct the shallow depressions of the face, of accidental origin or related to age (scars, wrinkles, chicken legs).Belotero Soft can also be used to touch up a previous correction made with Beloter Basic, immediately or a few weeks after the first injection.
Belotero Soft must be injected into the surface or medium dermis by a legally qualified doctor.Because the treatment is successful, the doctor must have previously been trained in injection techniques aimed at increasing the volume of skin tissues.It is also essential to operate in adequate aseptic conditions.Belotero Soft is therefore intended for use in a medical office.It should be injected into a healthy skin, not inflamed and disinfected.

The package contains 1 syringe preriempted by 1ml.

Belotero SOFT It presents itself in the form of isotonic gel, sterile, apoish, viscoelastic, clear, colorless and transparent and It is also available in the version with Lidocaine.
 
The use of Beloteria Soft is not recommended in the following cases:

- In case of hypersensitivity to hyaluronic acid,
- in case of autoimmune or diabetes diseases,
- In case of repeated angina,
- in case of acute joint rheumatism,
- in patients prepared for the keloids,
- in pregnant or breastfeeding women, breastfeeding,
- in people who are under the age of 18.
 
Components:
Sodium sodium ialuronate: 20 mg/ml;phosphate buffer pH 7 q.s.: 1, 0 ml.

The application of the product is reserved exclusively for professional health workers with adequate qualification.Therefore, any liability for uses or applications of the product made by subjects not qualified for health treatments is declined.

Belotero Lips Shape It is used to give volume and sublimate the upper and lower lips.It is a sterile, apoish, viscoelastic, colorless and transparent gel.It is composed of reticulated sodium hyaluronate of non -animal origin and supplied in a saline phosphate buffer.Beloterian Lips Shape contains 0, 3% of Lidocaine hydrochloride.It is an injectable and reabsorbable system, indicated to correct atrophic heads of the face and for remodeling the volume of soft tissues (e.g. volume of the lips, deep oral commissures).It is also suitable for the correction of atrophic face scars.The presence of lidocaine allows you to reduce local pain associated with gel injection, improving patient comfort.

Belotero Lips It is also available in version Contour.

Format: 1 syning to 0, sh ml

Beloterian Lips Shape contains hyaluronate of reticulated sodium (22, 5 mg/ml), lidocaine hydrochloride (3, 0 mg/ml).It is recommended to use one of the needles provided in the package.The use of needles 27 g ½ supplied is recommended as a lower diameter would require greater strength during the injection of the system.Beltero Lips Shape must be injected slowly.The amount of gel to be injecting depends on the area to be treated and the correction to be obtained.It is not necessary over correction.After the injection, perform a light massage on the treated area, for a uniform distribution of the product.The amount of gel to be injecting depends on the area to be treated and the correction to be obtained.It is not necessary to correct.After the injection, perform a light massage on the treated area, for a uniform distribution of the product.Assembly of the syringe for optimal use of Belostero Lips Contour, it is important that the needle is correctly inserted in the syringe.1) Keep the glass cylinder of the syringe firmly and the Luer - Lock adapter between the thumb and index.2) with the hand, challenge the protective cap and unscrew it.3) Push and rotate the needle on the syringe to the detention.Do not tighten excessively to prevent the luer - lock from moving and detaching from the syringe.4) Continuing to keep the Luer - Lock, remove the ego sheath.Conservation preserve at a temperature between 2 ° C and 25 ° C.Protect against light and frost.Avoid mechanical shock.Format the package contains: - an illustrative sheet;- a pre - filled syringe;- 2 traceability labels;- 2 disposable sterile needles.

Warnings do not inject in the blood vessels, in areas that present skin problems of 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 in progression.It is also recommended to carefully monitor these patients after injection.It is recommended not to inject to patients with an anamnesis of streptococcal infections and in patients predisposed to hypertrophic or keloid scars.It must not be used in association with other aesthetic medicine techniques such as delamination (peeling), dermobrasion or any other type of laser treatment, before complete healing the last treatment.Keep in mind that even if the healing is reached earlier than expected, Belotero Lips Shape must not be used before 2 weeks after the last treatment.Before use, check the integrity of the internal package and the expiry date of both the syringe and the needle.Do not use these products after the expiry date and if the package has been opened or damaged.Patients taking antitrombotic substances, such as aspirin or non -steroidal anti -inflammatory drugs, have a greater probability of developing reactions such as hematomas, nodules or bleeding in injection.In the case of patients with epilepsy, compromise of cardiac function, severe impairment of liver function or serious renal dysfunction or porphyria, the doctor must decide on a case -by -case basis whether to proceed with the injection of Beloterian Lips Shape depending on the nature of the disease and theongoing treatment.Doctors and athletes must take into account the fact that lidocaine can cause positive results to anti -doping tests.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 redeem and not reuse, due to the risks associated with these practices, including infections.The patient must avoid putting on makeup for at least 12 hours after treatment and must avoid Turkish saunas and bathrooms 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 health workers with adequate qualification.Therefore, any liability for uses or applications of the product made by subjects not qualified for health treatments is declined.

Belotero Balance (without lidocaine) It is a Merz product.It is supplied in disposable glass syringe, it is indicated for the increase in the volume of the skin tissue and allows you to increase the volume of the lips, especially the free margin, and correct facial depressions due to trauma or age through injections in areas of theface.

Packaging: 1 pre -cenpated glass of 1 ml glass.

Belotero Balance is also available in version With lidocaine. 

Features: isotonic gel, sterile, apoish, viscoelastic, clear, colorless and transparent.
Components: reticulated sodium hyaluronate: 22, 5 mg/ml;phosphate buffer pH 7 q.s. :.1, 0 ml

Belotero Balance is destined to be injected into the deep dermis by a legally qualified doctor and in adequate aseptic conditions.The application of the product is reserved exclusively for professional health workers with adequate qualification.Therefore, any liability for uses or applications of the product made by subjects not qualified for health treatments is declined.

Belotero Balance con Lidocaina It is a Merz product.It is supplied in disposable glass syringe, it is indicated for the increase in the volume of the skin tissue and allows you to increase the volume of the lips, especially the free margin, and correct facial depressions due to trauma or age through injections in areas of theface.

Contains a 1 ml glass preriempted syringe.

Belotero Balance with lidocaine is also available in version Without lidocaine.

This device is destined to be injected into the deep dermis by a legally qualified doctor.Because the treatment is successful, the doctor must have previously been trained in injection techniques aimed at increasing the volume of skin tissues.It is also essential to operate in adequate aseptic conditions.Belotero Balance with lidocaine is intended for use in a medical office and must be injected into a healthy skin, not inflamed and disinfected.

Characteristics: Isotonic gel, sterile, apoish, viscoelastic, clear, colorless and transparent.

Components: Sodium sodium hyaluronate: 25, 5 mg/ml;phosphate buffer pH 7 q.s.: 1, 0 ml;lidocaine.

The application of the product is reserved exclusively for professional health workers with adequate qualification.Therefore, any liability for uses or applications of the product made by subjects not qualified for health treatments is declined.

Belotero Revive It provides direct hydration that thanks to hyaluronic acid in synergy with glycerol helps to limit the formation of wrinkles, moisturizes the skin and redefines the structure of the skin for a younger and radiant appearance.

Belotero Revive determines all this with a natural touch, without drastic volume changes, and can be injected on several treatments giving a young brightness from the inside to the outside.

Format: 1 disposable 1 ml glass syringe.

Beloterian soft with lidocaine, 20 mg/ml of has cross-linkate, is indicated to increase the volume of the skin tissue that allows you to correct the shallow depressions of the face, of accidental origin or related to age (scars, wrinkles, chicken legs),to retouch a correction made with Beloteria Basic, immediately or a few weeks after the first injection.

Belotero Soft is also available in version Without lidocaine.

The application of the product is reserved exclusively for professional health workers with adequate qualification.Therefore, any liability for uses or applications of the product made by subjects not qualified for health treatments is declined.

Belotero Volume - 2 Siringhe of 1 ml

Si raccomanda il paziente di segnalare al proprio medico l‘insorgenza di qualsiasi effetto collaterale che duri più di una settimana. Il medico potrà infatti prescrivere al paziente un trattamento adeguato. Montaggio dell‘ago nella siringa Per un uso ottimale del prodotto, è importante che l‘ago sia correttamente inserito nella siringa. Si vedano i diagrammi 1, 2, 3 e 4. 1. Tenere saldamente il cilindro in vetro della siringa e l‘adattatore luer - lock tra pollice e indice. 2. Con l‘altra mano, afferrare il tappo protettivo e svitarlo. 3. Spingere e far ruotare l‘ago sulla siringa fi no al fermo. Non stringere eccessivamente per evitare che il luer - lock si sposti e si distacchi dalla siringa. 4. Continuando a tenere il luer - lock, rimuovere la guaina dall‘ago. Conservazione Conservare a una temperatura compresa tra 2°C e 30°C. Proteggere dalla luce e dal gelo. Evitare urti. Gel di ialuronato di sodio reticolato di origine non animale sterile, apirogeno, viscoelastico, incolore, trasparente, in un tampone fosfato salino. Presentazione Il prodotto viene fornito in una siringa preriempita monouso in vetro, sterilizzata con calore umido in autoclave. Ogni confezione contiene 2 siringhe di prodotto, 1 ago sterile 30G ½ Pollice e 1 ago sterile 27G ½, 1 cannula sterile 27 G/37 mm, 1 foglio illustrativo e 4 etichette di tracciabilità. Gli aghi sterili marcati CE sono monouso. Composizione Ialuronato di sodio reticolato 26 mg Tampone fosfato pH 7 q. s. Come riportato sull‘etichetta della siringa e sulla scatola. Il volume di gel contenuto in ogni siringa è riportato sull‘etichetta della siringa e sulla scatola. Il prodotto è un impianto iniettabile e riassorbibile, indicato per il ripristino dei volumi facciali, per esempio per aumentare il volume degli zigomi o del mento. Posologia e modo di somministrazione Il prodotto va utilizzato per iniezioni nel derma profondo, sottocute o nel periostio più esterno, da un medico debitamente abilitato allo svolgimento di questa procedura. Per il successo del trattamento è essenziale che il medico abbia ricevuto una formazione specifica sulle tecniche d‘iniezione per il ripristino del volume facciale. È necessario avere una buona conoscenza dell‘anatomia e della fisiologia del sito da trattare. Il trattamento va eseguito in condizioni di asepsi adeguate. Il prodotto deve essere iniettato in una pelle sana, non infiammata e disinfettata accuratamente in precedenza. Si raccomanda di utilizzare uno degli aghi forniti nella confezione. È tuttavia possibile usare altri aghi o cannule sterili che possono venire adattatti per il corretto collegamento al connettore luer - lock della siringa, in funzione della tecnica di iniezione adottata o delle preferenze del medico. In questo caso è possibile utilizzare un ago o una cannula raccomandati da Merz, con diametro compreso tra 18 G e 30 G. Per un uso ottimale del prodotto si raccomanda di eseguire il montaggio dell‘ago come illustrato nei diagrammi di seguito. Se l‘ago si ostruisce e la pressione dell‘iniezione diventa eccessiva, sospendere la procedura e cambiare l‘ago o la cannula. Se necessario, può essere utilizzato un anestetico locale o loco - regionale. In questo caso, è necessario attenersi alle istruzioni per l‘uso di questi prodotti. La quantità di gel da iniettare dipende dall‘area che deve essere sottoposta a trattamento. Si raccomanda di non iniettare, in una seduta, più di 3 ml per ogni sito di trattamento. Non sovracorreggere. Dopo l‘iniezione, eseguire un leggero massaggio sull‘area trattata, per una distribuzione uniforme del prodotto. Contro Il prodotto è controindicato nei seguenti casi: • ipersensibilità nota a uno o più dei componenti del prodotto, in particolare allo ialuronato di sodio; • nelle donne incinte e/o che allattano al seno; • nei giovani di età inferiore a 18 anni; • in pazienti che presentino un‘infezione generale. Non iniettare il prodotto nei vasi sanguigni. Non iniettare il prodotto nella regione glabellare. Non iniettare il prodotto nella regione dei solchi naso - giugali. Non iniettare il prodotto nelle labbra. Non iniettare il prodotto in aree che presentino problemi cutanei di natura infiammatoria o infettiva (acne, herpes, ecc. ). Non iniettare il prodotto per la correzione di rughe superficiali e rughe sottili (iniezione del prodotto nel derma superficiale). Non iniettare il prodotto in un‘area precedentemente trattata con filler dermico permanente. Precauzioni d‘uso Prima del trattamento, il paziente deve ricevere informazioni adeguate sul dispositivo, sulle contro e su eventuali effetti collaterali. In assenza di dati clinici sulla tollerabilità e sull‘efficacia delle iniezioni del prodotto nei pazienti con malattia autoimmune pregressa o in corso, il medico deve decidere caso per caso, a seconda della natura della malattia e del trattamento ricevuto, se procedere con l‘iniezione del prodotto. Si raccomanda di proporre a questi pazienti di sottoporsi a un doppio test preliminare e di non iniettare il prodotto se la malattia è in progressione. Si raccomanda inoltre di monitorare attentamente questi pazienti dopo l‘iniezione. Il prodotto può essere utilizzato per correggere i segni causati dalla perdita di tessuto adiposo facciale (lipoatrofia) in pazienti affetti da virus dell‘immunodeficienza umana. Si raccomanda di non iniettare il prodotto nei pazienti con un‘anamnesi di infezioni streptococciche e nei pazienti predisposti a cicatrici ipertrofiche o cheloidi. Si raccomanda di non iniettare il prodotto nella regione periorbitale. Il prodotto non deve essere utilizzato in associazione con altre tecniche di medicina estetica quali peeling, dermoabrasione o qualsiasi altro tipo di trattamento laser, prima della completa guarigione dell‘ultimo trattamento. In ogni caso, anche se si raggiunge la guarigione prima del previsto, il prodotto non deve essere utilizzato prima di 2 settimane dopo l‘ultimo trattamento. Non sono disponibili dati clinici sull‘uso combinato del prodotto con i trattamenti menzionati sopra. Non sono disponibili dati clinici sull‘iniezione del prodotto in una zona già trattata con un altro prodotto filler. Prima dell‘uso, verificare l‘integrità della confezione interna e la data di scadenza sia della siringa che dell‘ago. Non utilizzare questi prodotti dopo la data di scadenza o se la confezione risulta aperta o danneggiata. A discrezione del medico, può essere utilizzato un anestetico locale o loco - regionale. Tenere presente che l‘anestetico può causare arrossamento e ipersensibilità localizzati. I pazienti che assumono sostanze anticoagulanti, quali aspirina o farmaci antinfiammatori non steroidei, hanno una maggiore probabilità di sviluppare reazioni quali ematomi, noduli o sanguinamento in sede di iniezione. Non trasferire il prodotto in un altro contenitore e non aggiungere altri ingredienti al prodotto. Soltanto il gel, e non la superficie esterna della siringa, è sterile. Il prodotto non deve essere utilizzato con un dispositivo di iniezione automatico non raccomandato da Merz. Se si utilizza un dispositivo automatico, si raccomanda che il medico abbia precedentemente letto le istruzioni d‘uso del dispositivo di iniezione e che sia addestrato al suo utilizzo. Dopo l‘uso, gettare la siringa e il prodotto residuo. Non risterilizzare e non riutilizzare, a causa dei rischi associati a tali pratiche, comprese le infezioni. Il paziente deve evitare di applicare il trucco per almeno 12 ore dopo il trattamento e deve evitare saune e bagni turchi nonché un‘esposizione prolungata al sole o ai raggi UV per 2 settimane dopo il trattamento. I pazienti devono anche evitare di esercitare pressione e/o manipolare l‘area del viso trattata. Incompatibilità Lo ialuronato di sodio precipita in presenza di sali ammonici quaternari (quale il cloruro di benzalconio). È consigliabile quindi che il prodotto non entri in contatto con tali sostanze. Effetti collaterali Poiché potrebbero manifestarsi effetti collaterali, il medico deve informarne il paziente, prima del trattamento. Durante l‘iniezione potrebbe verificarsi un leggero sanguinamento che dovrebbe comunque scomparire spontaneamente al termine dell‘iniezione. In alcuni casi, subito dopo l‘iniezione o come reazione tardiva, potrebbero manifestarsi una o più delle seguenti reazioni (elenco non esaustivo): • reazioni solitamente associate all‘iniezione come arrossamento, eritema, edema o dolore, a volte accompagnate da prurito nell‘area trattata. Queste reazioni possono durare una settimana; - ematomi nell‘area trattata; - tumefazione nell‘area trattata; - indurimenti o noduli nell‘area trattata; - alterazioni del colore della pelle nell‘area trattata; - allergia a uno o più componenti del prodotto, in particolare allo ialuronato di sodio; - in letteratura sono stati riportati casi di necrosi, ascessi e granulomi dopo iniezioni di ialuronato di sodio. Tali rischi potenziali, benché rari, devono essere tenuti in considerazione.

Belotero volume with lidocaine is a filler containing sterile gel, apoish, viscoelastic, colorless and transparent.It is composed of reticulated sodium hyaluronate of non -animal origin and supplied as a saline phosphate buffer.The product contains 0.3% of the hydrochin hydrochloride.Belotero volume with Lido is specifically indicated to restore the volumes of the face.The hyaluronic acid -based filler is injected under the surface of the skin to give volume and smooth the unwanted wrinkles.The face fat, naturally present at birth, is gradually lost over time.This loss of volume can lead to the sagging of the skin, wrinkles and depressions in the face.This device is destined to be injected into the deep dermis by a legally qualified doctor.Because the treatment is successful, the doctor must have previously been trained in injection techniques aimed at increasing the volume of skin tissues.It is also essential to operate in adequate aseptic conditions.This product is intended for use in a medical office.It should be injected into a healthy and not inflamed skin, disinfected.Format: Pack of 2 Sirings of 1 ml

Descrizione
Biorepeelcl3 Fnd è un dispositivo medico brevettato, ad azione stimolante, rivitalizzante e peeling che promuove il turnover cellulare, rimuovendo le cellule più esterne dello strato corneo. Grazie alla presenza di principi attivi, Biorepeel cl3 contribuisce ad una profonda stimolazione di collagene e elastina e la veicolazione e l’assorbimento degli stessi come amminoacidi e vitamine consentono alla cute di rigenerarsi, idratarsi e dare alla pelle un aspetto migliore. Prodotto professionale destinato all’uso medico. Uso esterno.

Ingredienti/Inci
Acido tricoloroacetico, acido lactobionico, acido salicilico, acido tartarico, acido citrico, arginina, acido gamma-aminobutirrico, ascorbil glucoside, glicina, prolina, idrossiprolina, riboflavina.

Formato
Confezione 5 fiale da 6 ml

Minsan
907998999