Capito Glyfos Spray

Hauptinformation

  • Handelsname:
  • Capito Glyfos Spray
  • Darreichungsform:
  • AL Flüssigkeit zur unverdünnten Anwendung
  • 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:
  • Capito Glyfos Spray
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Herbizid

Weitere Informationen

Status

  • Quelle:
  • UFAG - Ufficio federale dell'agricoltura. OFAG - Office fédéral de l'agriculture. BLW - Bundesamt für Landwirtschaft.
  • Zulassungsnummer:
  • W-7015
  • Letzte Änderung:
  • 14-11-2018

Packungsbeilage: zusammensetzung, kinische angaben, nebenwirkungen, wechselwirkungen, dosierung, schwangerschaft, stillzeit

Handelsbezeichnung: Capito Glyfos Spray

Pflanzenschutzmittelverzeichnis (Stand: 06.11.2018)

Produktkategorie:

Bewilligungsinhaber:

Eidg. Zulassungsnummer:

Herbizid

Stähler Suisse SA

W-7015

Stoff(e):

Gehalt:

Formulierungscode:

Wirkstoff:

Glyphosat

0.72 % 7.2 g/l

[als 0.97% Glyphosat-

isopropylammoniumsalz (9.7 g / l)]

AL Flüssigkeit zur unverdünnten

Anwendung

Anwendungen

A

Kultur

Schaderreger/Wirkung

Dosierungshinweise

Auflagen

O Kernobst

Einjährige Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Gemeine Quecke

Aufwandmenge: 20 ml/m²

Anwendung: Gebrauchsfertig.

1, 2, 3, 4

O Kernobst

Mehrjährige Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 40 ml/m²

Anwendung: Gebrauchsfertig.

1, 2, 3, 4

Bäume und Sträucher

(ausserhalb Forst)

Einjährige Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Gemeine Quecke

Aufwandmenge: 20 ml/m²

Anwendung: Gebrauchsfertig.

1, 2, 3, 4

Bäume und Sträucher

(ausserhalb Forst)

Mehrjährige Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 40 ml/m²

Anwendung: Gebrauchsfertig.

1, 2, 3, 4

Z Blumenkulturen und

Grünpflanzen

Rosen

Zier- und Sportrasen

Einjährige Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 20 ml/m²

Anwendung:

Einzelpflanzenbehandlung.

Gebrauchsfertig.

1, 2, 3, 4

A

Kultur

Schaderreger/Wirkung

Dosierungshinweise

Auflagen

Gemeine Quecke

Blumenkulturen und

Grünpflanzen

Rosen

Zier- und Sportrasen

Mehrjährige Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 40 ml/m²

Anwendung:

Einzelpflanzenbehandlung.

Gebrauchsfertig.

1, 2, 3, 4

Z Brache

Einjährige Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Gemeine Quecke

Aufwandmenge: 20 ml/m²

Anwendung: Flächenbehandlung.

Gebrauchsfertig.

1, 2, 3, 4, 5

Z Brache

Mehrjährige Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 40 ml/m²

Anwendung: Gebrauchsfertig.

Flächenbehandlung.

1, 2, 3, 4, 5

Auflagen und Bemerkungen:

Nur im Hausgarten.

Keine Niederschläge während mindestens 6 Stunden nach der Behandlung.

Behandlung spätestens bis Ende August. Es dürfen keine grünen Teile der Kulturpflanzen mit dem

Herbizid in Kontakt kommen.

Bei der Anwendung des Mittels Schutzhandschuhe tragen.

Behandlung bis spätestens 2 Wochen vor der Saat oder Pflanzung.

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.

13-12-2018

Evaluation of the safety and efficacy of the organic acids lactic and acetic acids to reduce microbiological surface contamination on pork carcasses and pork cuts

Evaluation of the safety and efficacy of the organic acids lactic and acetic acids to reduce microbiological surface contamination on pork carcasses and pork cuts

Published on: Wed, 12 Dec 2018 Studies evaluating the safety and efficacy of lactic and acetic acids to reduce microbiological surface contamination on pork carcasses pre‐chill and pork meat cuts post‐chill were assessed. Lactic acid treatments consisted of 2–5% solutions at temperatures of up to 80°C applied to carcasses by spraying or up to 55°C applied on cuts by spraying or dipping. Acetic acid treatments consisted of 2–4% solutions at temperatures of up to 40°C applied on carcasses by spraying or o...

Europe - EFSA - European Food Safety Authority Publications

29-11-2018

Glyphosate: ANSES launches a comparative assessment with the available alternatives

Glyphosate: ANSES launches a comparative assessment with the available alternatives

Following the five-year re-approval of this active substance at European level in December 2017, ANSES is reassessing marketing authorisations for products containing glyphosate. For products for which an application for authorisation or re-authorisation has been submitted, the Agency will carry out a comparative assessment with the available alternatives. For each glyphosate-based product, all uses for which there is an alternative that meets the substitution criteria will therefore be prohibited.

France - Agence Nationale du Médicament Vétérinaire

19-11-2018

Certain Option and Personelle sunscreens voluntarily recalled because of bacterial contamination

Certain Option and Personelle sunscreens voluntarily recalled because of bacterial contamination

One lot each of Option Family Sunscreen Lotion SPF 50 and Personnelle Sport Sunscreen Lotion SPF 50 have been voluntarily recalled by Empack Spraytech Inc. because of bacterial contamination.

Health Canada

15-11-2018

Assessment of genetically modified maize MZHG0JG for food and feed uses, import and processing under Regulation (EC) No 1829/2003 (application EFSA‐GMO‐DE‐2016‐133)

Assessment of genetically modified maize MZHG0JG for food and feed uses, import and processing under Regulation (EC) No 1829/2003 (application EFSA‐GMO‐DE‐2016‐133)

Published on: Wed, 14 Nov 2018 The scope of application EFSA‐GMO‐DE‐2016‐133 is for food and feed uses, import and processing of genetically modified (GM) maize MZHG0JG in the European Union. Maize MZHG0JG was developed to confer tolerance to the herbicidal active substances glyphosate and glufosinate‐ammonium. The molecular characterisation data and bioinformatic analyses do not identify issues requiring food/feed safety assessment. None of the identified differences in the agronomic/phenotypic and com...

Europe - EFSA - European Food Safety Authority Publications

17-10-2018

Pest categorisation of Stagonosporopsis andigena

Pest categorisation of Stagonosporopsis andigena

Published on: Tue, 16 Oct 2018 00:00:00 +0200 The Panel on Plant Health performed a pest categorisation of Stagonosporopsis andigena, the causal agent of black blight of potato, for the EU. The pest is a well‐defined fungal species and reliable methods exist for its detection and identification. S. andigena is present in Bolivia and Peru. The pest is not known to occur in the EU and is listed in Annex IAI of Directive 2000/29/EC as Phoma andina, meaning its introduction into the EU is prohibited. The ma...

Europe - EFSA - European Food Safety Authority Publications

10-10-2018

Sprayology Issues Voluntary Nationwide Recall of Homeopathic Aqueous-Based Medicines Due to Microbial Contamination

Sprayology Issues Voluntary Nationwide Recall of Homeopathic Aqueous-Based Medicines Due to Microbial Contamination

Eight and Company LLC, d/b/a Sprayology is voluntarily recalling all lots within expiry from 10/18-7/22 of its aqueous-based homeopathic product line for human use. All products manufactured by the contract manufacturer, King Bio, have been recalled due to possible microbial contamination.

FDA - U.S. Food and Drug Administration

11-9-2018

Assessment of occupational and dietary exposure to pesticide residues

Assessment of occupational and dietary exposure to pesticide residues

Published on: Mon, 27 Aug 2018 00:00:00 +0200 Plant protection products (PPPs) are pesticides containing at least one active substance that drives specific actions against pests (diseases). PPPs are regulated in the EU and cannot be placed on the market or used without prior authorisation. EFSA assesses the possible risks of the use of active substances to humans and environment. Member States decide whether or not to approve their use at EU level. Furthermore, Member States decide at national level on ...

Europe - EFSA - European Food Safety Authority Publications

17-8-2018

Empack Spraytech Inc. recalls Emzone Brake & Parts Cleaner

Empack Spraytech Inc. recalls Emzone Brake & Parts Cleaner

The products were designed and labelled for professional/trade (GHS) requirements and should have only been sold to industrial clients. However, these products were sold to industrial and retail clients. The professional grade product, which lacks consumer labelling information, including appropriate warnings, may lead to serious injury or property damage.

Health Canada

31-5-2018

Fluticasone Propionate Nasal Spray by Apotex Corp: Recall - Due to Potential for Small Glass Particles

Fluticasone Propionate Nasal Spray by Apotex Corp: Recall - Due to Potential for Small Glass Particles

The glass particles could block the actuator and impact the functionality of the pump and expose patients to the glass particles.

FDA - U.S. Food and Drug Administration

31-5-2018

Apotex Corp. Issues Voluntary Nationwide Recall of Fluticasone Propionate Nasal Spray USP 50 mcg Per Spray 120 Metered Sprays Due to Potential for Small Glass Particles

Apotex Corp. Issues Voluntary Nationwide Recall of Fluticasone Propionate Nasal Spray USP 50 mcg Per Spray 120 Metered Sprays Due to Potential for Small Glass Particles

Apotex Corp. is voluntarily recalling one (1) lot of Fluticasone Propionate Nasal Spray, USP, 50 mcg per spray, 120 Metered Sprays, to the consumer level. The Fluticasone Propionate Nasal Spray USP 50 mcg per spray 120 Metered Sprays has been found to contain small glass particles. The glass particles could block the actuator and impact the functionality of the pump. The issue was discovered through a customer complaint.

FDA - U.S. Food and Drug Administration

25-5-2018

Safe use of personal insect repellents

Safe use of personal insect repellents

While enjoying the warm summer weather, don't forget to protect yourself from pesky bugs that bite! Health Canada is reminding Canadians to use bug spray and other insect repellents safely to avoid mosquito and other bug bites.

Health Canada

22-5-2018

Koi Med Anti Pilz ad us. vet., Spray

Koi Med Anti Pilz ad us. vet., Spray

● Die Zulassung ist am 22.05.2018 erloschen.

Institut für Veterinärpharmakologie und toxikologie

21-5-2018

Homeopathic Teething Drops, Nausea Drops, Intestinal Colic Drops, Stomach Calm, Expectorant Cough Syrup, Silver-Zinc Throat Spray, and Argentum Elixir by MBI Distributing: Recall - Due to a Lack of Adequate Controls

Homeopathic Teething Drops, Nausea Drops, Intestinal Colic Drops, Stomach Calm, Expectorant Cough Syrup, Silver-Zinc Throat Spray, and Argentum Elixir by MBI Distributing: Recall - Due to a Lack of Adequate Controls

Manufacturing products without proper process controls increases the probability that products will vary in strength, quality and purity

FDA - U.S. Food and Drug Administration

18-5-2018

MBI Distributing, Inc. Issues Voluntary Nationwide Recall of Homeopathic Teething Drops, Nausea Drops, Intestinal Colic Drops, Stomach Calm, Expectorant Cough Syrup, Silver-Zinc Throat Spray, and Argentum Elixir Due to a Lack of Process Controls

MBI Distributing, Inc. Issues Voluntary Nationwide Recall of Homeopathic Teething Drops, Nausea Drops, Intestinal Colic Drops, Stomach Calm, Expectorant Cough Syrup, Silver-Zinc Throat Spray, and Argentum Elixir Due to a Lack of Process Controls

MBI Distributing, Inc. is voluntarily recalling all lots of homeopathic Teething Drops, Nausea Drops, Intestinal Colic Drops, Stomach Calm, Expectorant Cough Syrup, Silver-Zinc Throat Spray, and Argentum Elixir, within expiry, to the consumer level. The drug products have been found to be manufactured with a lack of adequate controls.

FDA - U.S. Food and Drug Administration

8-5-2018

Koi Med Wound Spray ad us. vet.

Koi Med Wound Spray ad us. vet.

● Die Zulassung ist am 08.05.2018 erloschen.

Institut für Veterinärpharmakologie und toxikologie

14-1-2019

Nitrolingual® Nitrospray

Rote - Liste

30-11-2018

Azedil 1 mg/ml Nasenspray

Rote - Liste

19-11-2018

Mirfulan® Spray N

Rote - Liste

16-11-2018

Panthenol Spray

Rote - Liste

30-10-2018

Nitrolingual® Spray

Rote - Liste

14-9-2018

Nitrolingual akut® Spray

Rote - Liste

3-9-2018

Echinacea Mund- und Rachenspray

Rote - Liste

11-7-2018

Terbinafin HCL acis 10 mg/g Spray

Rote - Liste

10-7-2018

Lamisil® Spray

Rote - Liste

10-7-2018

Otriven® SinuSpray 0,1%

Rote - Liste

10-7-2018

Otri-Allergie Nasenspray Fluticason

Rote - Liste

10-5-2018

Inhalation and nasal spray registered medicines

Inhalation and nasal spray registered medicines

New information about application pathways and data requirements for inhalation and nasal spray registered medicines

Therapeutic Goods Administration - Australia