Input classic

Hauptinformation

  • Handelsname:
  • Input classic
  • Verwenden für:
  • Pflanzen
  • Art der Medizin:
  • Agrochemisch

Dokumenten

  • Information für medizinisches Fachpersonal:
  • Das Informationsblatt für dieses Produkt ist derzeit nicht verfügbar, können Sie eine Anfrage an unseren Kundendienst zu senden und wir werden Sie benachrichtigen, sobald wir in der Lage, um es zu erhalten.


    Fordern Sie die Packungsbeilage für medizinisches Fachpersonal.

Lokalisierung

  • Erhältlich in:
  • Input classic
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Fungizid

Weitere Informationen

Status

  • Quelle:
  • UFAG - Ufficio federale dell'agricoltura. OFAG - Office fédéral de l'agriculture. BLW - Bundesamt für Landwirtschaft.
  • Zulassungsnummer:
  • D-4256
  • Letzte Änderung:
  • 06-09-2017

Packungsbeilage

Produkt:

Handelsbezeichnung: Input classic (Parallelimport)

Produktekategorie

Ausl. Bewilligungsinhaber Eidg. Zulassungsnummer

Fungizid

Bayer CropScience AG

D-4256

Packungsbeilagenummer

Herkunftsland

Ausl. Zulassungsnummer

7339

Deutschland

5625-00

Stoff(e)

Gehalt

Formulierungscode

Wirkstoff: Spiroxamine

30.5 % 300 g/l

EC Emulsionskonzentrat

Wirkstoff:

Prothioconazole

16.3 % 160 g/l

Anwendungen

A Kultur

Schaderreger/Wirkung

Dosierungshinweise

Auflagen

F Gerste

Echter Mehltau des Getreides

Netzfleckenkrankheit der Gerste

Rhynchosporium-Blattfleckenkrankheit

Sprenkelnekrosen (PLS+RCC)

Zwergrost der Gerste

Aufwandmenge: 0.75 l/ha

Anwendung: Stadium 31-51

(BBCH).

1, 2, 3, 4, 5

F Gerste

Echter Mehltau des Getreides

Netzfleckenkrankheit der Gerste

Rhynchosporium-Blattfleckenkrankheit

Sprenkelnekrosen (PLS+RCC)

Zwergrost der Gerste

Aufwandmenge: 1.25 l/ha

Anwendung: Stadium 31-51

(BBCH).

1, 2, 4, 5

Korn

(Dinkel)

Braunrost

Echter Mehltau des Getreides

Septoria-Blattdürre (S. tritici oder S.

nodorum)

Aufwandmenge: 1.25 l/ha

Anwendung: Stadium 31-61

(BBCH).

1, 4, 5

F Korn

(Dinkel)

Braunrost

Echter Mehltau des Getreides

Septoria-Blattdürre (S. tritici oder S.

Aufwandmenge: 0.75 l/ha

Anwendung: Stadium 31-61

1, 3, 4, 5

A Kultur

Schaderreger/Wirkung

Dosierungshinweise

Auflagen

nodorum)

(BBCH).

Triticale

Weizen

Ährenfusariosen

Aufwandmenge: 1.25 l/ha

Anwendung: Stadium 55-69

(BBCH).

1, 4, 5

F Triticale

Braunrost

Echter Mehltau des Getreides

Gelbrost

Rhynchosporium-Blattfleckenkrankheit

Septoria-Blattdürre (S. tritici oder S.

nodorum)

Aufwandmenge: 0.75 l/ha

Anwendung: Stadium 31-61

(BBCH).

1, 3, 4, 5

F Triticale

Braunrost

Echter Mehltau des Getreides

Gelbrost

Septoria-Blattdürre (S. tritici oder S.

nodorum)

Aufwandmenge: 1.25 l/ha

Anwendung: Stadium 31-61

(BBCH).

1, 4, 5

F Weizen

Braunrost

Echter Mehltau des Getreides

Gelbrost

Septoria-Blattdürre (S. tritici oder S.

nodorum)

Septoria-Spelzenbräune (S. nodorum)

Aufwandmenge: 0.65 l/ha

Anwendung: Stadium 31-61

(BBCH).

1, 4, 5, 7

F Weizen

Braunrost

Echter Mehltau des Getreides

Gelbrost

Septoria-Blattdürre (S. tritici oder S.

nodorum)

Septoria-Spelzenbräune (S. nodorum)

Sprenkelnekrosen (PLS)

Aufwandmenge: 1.25 l/ha

Anwendung: Stadium 31-61

(BBCH).

1, 4, 5, 6

F Weizen

Halmbruchkrankheit des Getreides

Aufwandmenge: 1.25 l/ha

Anwendung: Stadium 30-32

(BBCH).

1, 4, 5

F Weizen

Halmbruchkrankheit des Getreides

Aufwandmenge: 0.65 l/ha

Anwendung: Stadium 30-32

(BBCH).

1, 4, 5, 7

F Winterroggen

Braunrost

Rhynchosporium-Blattfleckenkrankheit

Septoria-Blattdürre (S. tritici oder S.

nodorum)

Aufwandmenge: 0.75 l/ha

Anwendung: Stadium 37-61

(BBCH).

1, 3, 4, 5

F Winterroggen

Braunrost

Rhynchosporium-Blattfleckenkrankheit

Septoria-Blattdürre (S. tritici oder S.

nodorum)

Aufwandmenge: 1.25 l/ha

Anwendung: Stadium 37-61

(BBCH).

1, 4, 5

Auflagen und Bemerkungen:

Maximal 1 Behandlung pro Kultur.

PLS+RCC = Physiological Leaf Spots und Ramularia collo-cygni.

In Tankmischung mit 0.75 l/ha Fandango.

SPe 3: Zum Schutz von Gewässerorganismen vor den Folgen von Drift eine unbehandelte

Pufferzone von 20 m zu Oberflächengewässern einhalten. Zum Schutz vor den Folgen einer

Abschwemmung eine mit einer geschlossenen Pflanzendecke bewachsene Pufferzone von

mindestens 6 m einhalten. Reduktion der Distanz aufgrund von Drift und Ausnahmen gemäss den

Weisungen des BLW.

Ansetzen der Spritzbrühe: Schutzhandschuhe + Schutzbrille oder Visier tragen. Ausbringen der

Spritzbrühe: Schutzhandschuhe + Schutzanzug tragen. Technische Schutzvorrichtungen während

des Ausbringens (z.B. geschlossene Traktorkabine) können die vorgeschriebene persönliche

Schutzausrüstung ersetzen, wenn gewährleistet ist, dass sie einen vergleichbaren oder höheren

Schutz bieten.

PLS = Physiological Leaf Spots

In Tankmischung mit 0.65 l/ha Fandango.

Gefahrenkennzeichnungen:

Es gilt die Einstufung und Kennzeichnung der ausländischen Originaletikette.

Zusätzliche Schweizerische Gefahrenkennzeichnungen:

SP 1 Mittel und/oder dessen Behälter nicht in Gewässer gelangen lassen.

Im Zweifelsfall gelten einzig die Originaldokumente der Zulassung. Die Erwähnung eines Produktes,

Wirkstoffes oder einer Firma stellt keine Empfehlung dar und bedeutet nicht, dass sich das Produkt im

Verkauf befindet.

19-10-2018

Core Health & Fitness recalls Stairmaster 8G Gauntlet Stepmill Machines

Core Health & Fitness recalls Stairmaster 8G Gauntlet Stepmill Machines

The steps can accelerate rapidly without input from the user, posing a fall hazard.

Health Canada

17-10-2018

Applicability of in silico tools for the prediction of dermal absorption for pesticides

Applicability of in silico tools for the prediction of dermal absorption for pesticides

Published on: Tue, 16 Oct 2018 00:00:00 +0200 Based on the “Human in vitro dermal absorption datasets” published as supporting information to the revised EFSA Guidance on Dermal Absorption, in silico models for prediction of absorption across the skin have been evaluated. For this evaluation, a systematic literature search and review was performed, identifying 288 publications describing mathematical models for prediction of dermal absorption. Eleven models potentially relevant to the regulatory assessm...

Europe - EFSA - European Food Safety Authority Publications

29-8-2018

Outcome of the public consultation on a draft protocol for the Scientific Opinion on dietary sugars

Outcome of the public consultation on a draft protocol for the Scientific Opinion on dietary sugars

Published on: Fri, 10 Aug 2018 00:00:00 +0200 The European Food Safety Authority (EFSA) carried out a public consultation to receive input from the scientific community and all interested parties on a draft protocol for the Scientific Opinion on free sugars from all dietary sources, prepared by the EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA Panel), supported by the ad‐hoc Working Group on Sugars. The draft protocol was endorsed by the Panel for public consultation at its plenary meeti...

Europe - EFSA - European Food Safety Authority Publications

29-8-2018

Safety assessment of the process ‘General Plastic’, based on Starlinger Decon technology, used to recycle post‐consumer PET into food contact materials

Safety assessment of the process ‘General Plastic’, based on Starlinger Decon technology, used to recycle post‐consumer PET into food contact materials

Published on: Fri, 10 Aug 2018 00:00:00 +0200 This scientific opinion of the EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF Panel) deals with the safety evaluation of the recycling process General Plastic (EU register No RECYC153), which is based on the Starlinger Decon technology. The decontamination efficiency of the process was demonstrated by a challenge test. The input of this process is hot caustic washed and dried poly(ethylene terephthalate) (PET) flakes orig...

Europe - EFSA - European Food Safety Authority Publications

29-8-2018

Update of the tolerable upper intake level for vitamin D for infants

Update of the tolerable upper intake level for vitamin D for infants

Published on: Tue, 07 Aug 2018 00:00:00 +0200 The European Food Safety Authority (EFSA) carried out a public consultation to receive input from the scientific community and all interested parties on the draft Scientific Opinion on the update of the tolerable upper intake level for vitamin D for infants. This draft Scientific Opinion was prepared by the EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA Panel) and endorsed by the Panel for public consultation by written procedure on 9 April 20...

Europe - EFSA - European Food Safety Authority Publications

26-6-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s new steps to advance health through improvements in nutrition under the agency’s Nutrition Innovation Strategy

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA’s new steps to advance health through improvements in nutrition under the agency’s Nutrition Innovation Strategy

Announcement of public meeting to solicit input on plans to modernize food standards and labeling

FDA - U.S. Food and Drug Administration

5-6-2018

Dringende Sicherheitsinformation zu OmniDiagnost Classic -  OmniDiagnost-Eleva von Philips Medical Systems Nederland B.V

Dringende Sicherheitsinformation zu OmniDiagnost Classic - OmniDiagnost-Eleva von Philips Medical Systems Nederland B.V

Weitere Informationen sowie Details zum Produkt entnehmen Sie bitte der anliegenden Kundeninformation des Herstellers.

Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

29-5-2018

Résultats ILPT Classical Swine Fever SEROLOGY 2018

Résultats ILPT Classical Swine Fever SEROLOGY 2018

France - Agence Nationale du Médicament Vétérinaire

23-5-2018

The FDA is Seeking Input on the Evaluation of Approaches to Demonstrate Effectiveness of Heartworm Preventatives for Dogs

The FDA is Seeking Input on the Evaluation of Approaches to Demonstrate Effectiveness of Heartworm Preventatives for Dogs

FDA’s CVM is evaluating the design of studies intended to support the standard of effectiveness for new animal drugs to prevent heartworm disease in dogs. The FDA is requesting public input on evaluating these products to assist in the potential development of alternative study designs.

FDA - U.S. Food and Drug Administration

25-9-2018

We hope this extra time will allow stakeholders to continue to provide  input on the ideas shared during the two-day Pediatric Device  Development public meeting held last month. #devices4kids https://go.usa.gov/xPjwd 

We hope this extra time will allow stakeholders to continue to provide input on the ideas shared during the two-day Pediatric Device Development public meeting held last month. #devices4kids https://go.usa.gov/xPjwd 

We hope this extra time will allow stakeholders to continue to provide input on the ideas shared during the two-day Pediatric Device Development public meeting held last month. #devices4kids https://go.usa.gov/xPjwd 

FDA - U.S. Food and Drug Administration

17-9-2018

 European Medicines Agency (EMA) Human Scientific Committees' Working Parties with Patients’ and Consumers’ Organisations (PCWP), European Medicines Agency, London, UK, From: 25-Sep-2018, To: 25-Sep-2018

European Medicines Agency (EMA) Human Scientific Committees' Working Parties with Patients’ and Consumers’ Organisations (PCWP), European Medicines Agency, London, UK, From: 25-Sep-2018, To: 25-Sep-2018

This Patients' and Consumers' Working Party (PCWP) plenary meeting will include discussions on patient engagement along the regulatory lifecycle and visibility of patient input throughout scientific procedures. Feedback will also be given from the representatives of the Scientific Committees.

Europe - EMA - European Medicines Agency

9-8-2018

Consultation: Proposed therapeutic goods advertising code guidance

Consultation: Proposed therapeutic goods advertising code guidance

The TGA is seeking input from interested parties on the revised version of the guidance to support the Code. Closing date: 4 October 2018

Therapeutic Goods Administration - Australia

7-8-2018

Dorithricin® Halstabletten Classic

Rote - Liste

18-7-2018

HSCC announced today a new workstream, conducted under the Task Group, that will discuss and seek input on a software bill of materials (SBOM) for medical devices. SBOMs can ensure that users have better understanding of what software elements are in a me

HSCC announced today a new workstream, conducted under the Task Group, that will discuss and seek input on a software bill of materials (SBOM) for medical devices. SBOMs can ensure that users have better understanding of what software elements are in a me

HSCC announced today a new workstream, conducted under the Task Group, that will discuss and seek input on a software bill of materials (SBOM) for medical devices. SBOMs can ensure that users have better understanding of what software elements are in a medical device.

FDA - U.S. Food and Drug Administration

19-6-2018

New information about #FDAPrecert and opportunity for public input now available-  https://go.usa.gov/xQJmG  #DigitalHealth #MedicalDevice #mhealth

New information about #FDAPrecert and opportunity for public input now available- https://go.usa.gov/xQJmG  #DigitalHealth #MedicalDevice #mhealth

New information about #FDAPrecert and opportunity for public input now available- https://go.usa.gov/xQJmG  #DigitalHealth #MedicalDevice #mhealth

FDA - U.S. Food and Drug Administration