CHF 18.25

1-24 hours

Delivery is possible through one of our partner pharmacies after consultation.

Swissmedic Nr.: 36566019
Index: 10.05.20

Pharmacode: 625421
GTIN/EAN: 7680365660199
Markteintritt: 12.07.1972

Kategorie: B Mehrmalige Abgabe auf eine ärztliche Verschreibung hin.


Kenacort® A Tinktur (22 mg)

Triamcinolon (D07XB02)

15 ml

(0/5 , 252)

Um Kenacort® A Tinktur (22 mg) kaufen zu können, benötigen Sie zunächst ein Rezept. Bei Deindoktor.ch können Sie im Rahmen einer Online-Sprechstunde per Webcam, mit dem Artz Ihrer Wahl, ein elektronische Rezept erhalten.

Das mit DeinDoktor.ch erhaltene Rezept kann in einer der 1400 Schweizer Apotheken verwendet werden. Wir organisieren mit einer unserer Partner-Apotheken eine Sendung Ihres Kenacort® A Tinktur (22 mg)'s gegen Unterschrift (24h) oder dem Medikamenten-Taxi nach einer Online Sprechstunde, falls gewünscht.


No doctor is now available for video consultation.
Your received prescription through DeinDoktor.ch is usable to get your medicaments in any of the 1400 Swiss pharmacies or in the Swiss online pharmacies. We can arrange with one of our pharmacy-partners a delivery against signature (24h) or medicament-taxi after an online-consultation.

Kenacort A Tinktur ist ein Arzneimittel zur Behandlung entzündlicher Erkrankungen der Haut. Sie enthält als Wirkstoff ein Kortikosteroid.

Kenacort A hemmt die Entzündung, lindert Juckreiz und Brennen und wirkt gegen die Allergie. Kenacort A erhalten Sie auf Verschreibung des Arztes oder der Ärztin.

Kenacort A wird auf der Haut angewendet bei:

akuten und chronischen, entzündlichen, auf Kortikosteroide ansprechenden Hautkrankheiten wie z.B. Psoriasis (Schuppenflechte), Ekzeme verschiedener Ursache.

Die Tinktur eignet sich vor allem für die Behandlung von sichtbaren Hautpartien und des Haarbodens sowie an schwer zugänglichen Stellen (z.B. Kopfhaut und Nägel).

Wenn Sie auf einen der Inhaltsstoffe überempfindlich reagieren, dürfen Sie Kenacort A nicht anwenden. Eine Behandlung mit Kenacort A ist für Sie ebenfalls nicht geeignet bei Akne, Hauttuberkulose, Virusinfektionen (z.B. Windpocken, Gürtelrose, Fieberbläschen) sowie bei Infektionen der Haut mit Pilzen oder Bakterien.

Das Präparat darf nicht in den Gehörgang gebracht werden.

Kenacort A ist ein stark wirksames Arzneimittel. Überschreiten Sie nicht die vom Arzt oder von der Ärztin vorgeschriebene Behandlungsdauer, da sich sonst Hautschäden einstellen können.

Wenn eine Hautkrankheit nicht innert einiger Tage auf die Behandlung anspricht oder sich gar verschlimmert, konsultieren Sie Ihren Arzt oder Ihre Ärztin. Teilen Sie ihm bzw. ihr ebenfalls mit, wenn Juckreiz und Rötung, Bläschen oder eine starke Verdünnung der Haut und Verletzungen auftreten.

Eine grossflächige Anwendung (mehr als 10% der Körperoberfläche) sowie eine Anwendung auf verstärkt resorbierenden Hautarealen (offenen Wunden, geschädigter Haut, intertriginösen Bereichen [Hautfalten] in Gelenkbeugen sowie zwischen den Fingern bzw. Zehen, Haut/Schleimhautgrenzen, um die Augen herum) ist zu vermeiden.

Am Gesicht, in der Leistengegend und in den Achselhöhlen ist die Anwendung von Kenacort A über längere Zeit zu vermeiden. Kenacort A darf nicht mit den Augen in Berührung kommen. Verwenden Sie Kenacort A nur für Ihr jetziges Hautleiden, für das der Arzt oder die Ärztin es Ihnen verschrieben hat, nicht aber für andere spätere Hautleiden. Geben Sie Kenacort A nicht an andere Personen weiter.

Informieren Sie Ihren Arzt oder Apotheker bzw. Ihre Ärztin oder Apothekerin, wenn Sie an anderen Krankheiten (speziell Diabetes, Tuberkulose, Magengeschwür) leiden, Allergien haben oder andere Arzneimittel (auch selbstgekaufte) einnehmen oder äusserlich anwenden!

Während der Schwangerschaft sollte Kenacort A nur auf ausdrückliche ärztliche Verordnung, nicht grossflächig und nicht während langer Zeit aufgetragen werden. Bei der Anwendung an den Brüsten soll nicht gestillt werden. Informieren Sie Ihren Arzt bzw. Ihre Ärztin, wenn Sie schwanger sind, es werden möchten oder stillen.

Wenn vom Arzt oder von der Ärztin nicht anders verordnet, gelten folgende Richtlinien:

Auf der Haut

Erwachsene (Patienten ab dem 18. Lebensjahr):

Die Tinktur 1?2× täglich sanft auf der befallenen Hautstelle verreiben.

Die Dauer der Behandlung wird individuell von Ihrem Arzt bzw. Ihrer Ärztin festgelegt.

Falls von Ihrem Arzt bzw. Ihrer Ärztin empfohlen, kann über die eingetrocknete Tinktur eine nicht zu dünne Schicht Fettsalbe aufgetragen werden.

Die Anwendung und Sicherheit von Kenacort A bei Kindern und Jugendlichen ist bisher nicht geprüft worden und kann daher bei Personen <18 Jahren nicht empfohlen werden.

Ändern Sie nicht von sich aus die verschriebene Dosierung. Wenn Sie glauben, das Arzneimittel wirke zu schwach oder zu stark, so sprechen Sie mit Ihrem Arzt oder Apotheker bzw. mit Ihrer Ärztin oder Apothekerin.

Folgende Nebenwirkungen können bei der Anwendung von Kenacort A auftreten:

Lokale unerwünschte Wirkungen wie Reizungen der Haut, Brennen, Jucken und Trockenheit sowie Überempfindlichkeitsreaktionen können auftreten. Die Behandlung mit Kenacort A kann zu Hautveränderungen wie Verdünnung der behandelten Hautstellen, zu Erweiterungen kleiner oberflächlicher Blutgefässe und zur Bildung von blau-rötlichen Streifen führen, besonders bei längerer Therapiedauer am Gesicht, in der Leistengegend, unter den Achselhöhlen oder unter Deckverbänden. Lokale Unverträglichkeitserscheinungen (z.B. starke Rötung, Brennen, Jucken) sind selten (<1/1000, ?1/10?000).

Falls Sie während der Behandlung eine Verschlechterung der Hauterkrankung feststellen, teilen Sie dies Ihrem Arzt oder Ihrer Ärztin mit.

Bei der Anwendung von Kenacort A unter Deckverbänden sind in seltenen Fällen (<1/1000, ?1/10?000) Schwindelgefühl und Schwäche beobachtet worden. Treten solche Anzeichen bei Ihnen auf, informieren Sie Ihren Arzt oder Ihre Ärztin.

Wenn Sie Nebenwirkungen bemerken, die hier nicht beschrieben sind, sollten Sie Ihren Arzt oder Apotheker bzw. Ihre Ärztin oder Apothekerin informieren.

Das Arzneimittel darf nur bis zu dem auf dem Behälter mit «EXP» bezeichneten Datum verwendet werden.

Kenacort A soll bei Raumtemperatur (15?25 °C), ausserhalb der Reichweite von Kindern aufbewahrt werden.

Nach Anbruch 6 Monate haltbar.

Wenn die Tinktur beim Auftragen brennt, soll nach dem letzten Eintrocknen etwas Fettsalbe auf die behandelte Stelle aufgetragen werden.

Weitere Auskünfte erteilt Ihnen Ihr Arzt oder Apotheker bzw. Ihre Ärztin oder Apothekerin. Diese Personen verfügen über die ausführliche Fachinformation.

1 g Kenacort A Tinktur enthält Triamcinolonacetonid 2 mg, Salicylsäure 20 mg, Alkohol sowie weitere Hilfsstoffe.

36566 (Swissmedic).

In Apotheken nur gegen ärztliche Verschreibung.

Kenacort A Tinktur: Plastiktropfflasche à 15 ml und 50 ml.

Dermapharm AG, Hünenberg.

Diese Packungsbeilage wurde im Juni 2015 letztmals durch die Arzneimittelbehörde (Swissmedic) geprüft.

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Evaluate medicament: Kenacort® A Tinktur (22 mg)


Write about your experience with the medicament. Share your experiences about the medication which you are currently taking or have taken. This information will help others. Thank you for your participation!
How effective was the medicament? (1: not effective, 5: very effective)
How easy was the medicament to use? (1: not easy, 5: very easy)
Would you recommend someone else to use this medicament? (1: would never recommend, 5: would definitely recommend)
How many effects caused the medicament? (1: lots of side effects, 5: no side effects)
How heavy were the side effects caused by the medicament? (1: very heavy, 5: not heavy)
I hereby certify that all information is true and accurate. My evaluation reflects my personal experience. My evaluation is appropriate and serves to benefit others before usage of the medicament.