Solado Gold

Hauptinformation

  • Handelsname:
  • Solado Gold
  • Darreichungsform:
  • SL Wasserlösliches Konzentrat
  • 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:
  • Solado Gold
    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:
  • I-2074
  • Letzte Änderung:
  • 15-11-2018

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

Handelsbezeichnung: Solado Gold

(Parallelimport)

Pflanzenschutzmittelverzeichnis (Stand: 06.11.2018)

Produktkategorie:

Ausl. Bewilligungsinhaber:

Eidg. Zulassungsnummer:

Herbizid

Monsanto agricoltura Italia S.p.A.

I-2074

Stoff(e):

Gehalt:

Formulierungscode:

Wirkstoff: Glyphosat

30.8 % 360 g/l

[als 41.5% Glyphosat-isopropylammoniumsalz

(486 g/l)]

SL Wasserlösliches

Konzentrat

Anwendungen

A

Kultur

Schaderreger/

Wirkung

Dosierungshinweise

Auflagen

B Brombeere

Einjährige

Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Gemeine Quecke

Aufwandmenge: 2 - 3 l/ha

1, 2, 3

B Brombeere

Mehrjährige

Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 4 - 10 l/ha

1, 2, 3

Kernobst

Steinobst

Einjährige

Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Gemeine Quecke

Aufwandmenge: 2 - 3 l/ha

1, 2, 3

O Kernobst

Steinobst

Mehrjährige

Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

Aufwandmenge: 4 - 10 l/ha

1, 2, 3

A

Kultur

Schaderreger/

Wirkung

Dosierungshinweise

Auflagen

(Ungräser)

W Ertragsreben

Einjährige

Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Gemeine Quecke

Aufwandmenge: 2 - 3 l/ha

1, 2, 3

W Ertragsreben

Mehrjährige

Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 4 - 10 l/ha

1, 2, 3

G Brache

Einjährige

Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Gemeine Quecke

Aufwandmenge: 2 - 3 l/ha

1, 2, 4

G Brache

Mehrjährige

Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 4 - 10 l/ha

1, 2, 4

Brache

Einjährige

Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Gemeine Quecke

Aufwandmenge: 2 - 3 l/ha

1, 2, 4

Brache

Mehrjährige

Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 4 - 10 l/ha

1, 2, 4

Mais

Einjährige

Dicotyledonen

(Unkräuter)

Einjährige

Aufwandmenge: 2 - 3 l/ha

Anwendung: Bei der Saat.

1, 2, 5, 6

A

Kultur

Schaderreger/

Wirkung

Dosierungshinweise

Auflagen

Monocotyledonen

(Ungräser)

Gemeine Quecke

Mais

Mehrjährige

Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 4 - 10 l/ha

Anwendung: Bei der Saat.

1, 2, 5, 6

Wiesen und Weiden

Dicotyledonen

(Unkräuter)

Monocotyledonen

(Ungräser)

Aufwandmenge: 4 - 10 l/ha

Anwendung:

Flächenbehandlung; vor

Neuansaat.

1, 2, 4

Wiesen und Weiden

Dicotyledonen

(Unkräuter)

Monocotyledonen

(Ungräser)

Konzentration: 5 - 10 %

Wartefrist: 3 Woche(n)

Anwendung:

Einzelpflanzenbehandlung mit

Handspritzgeräten.

1, 2, 7

Wiesen und Weiden

Dicotyledonen

(Unkräuter)

Monocotyledonen

(Ungräser)

Konzentration: 0.5 - 1.5 %

Wartefrist: 3 Woche(n)

Anwendung:

Einzelpflanzenbehandlung mit

Rückenspritze.

1, 2, 7

Bäume und Sträucher

(ausserhalb Forst)

Rosen

Einjährige

Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Gemeine Quecke

Aufwandmenge: 2 - 3 l/ha

1, 2, 3

Bäume und Sträucher

(ausserhalb Forst)

Rosen

Mehrjährige

Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 4 - 10 l/ha

1, 2, 3

Brache

Einjährige

Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Gemeine Quecke

Aufwandmenge: 2 - 3 l/ha

1, 2, 4

A

Kultur

Schaderreger/

Wirkung

Dosierungshinweise

Auflagen

Brache

Mehrjährige

Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 4 - 10 l/ha

1, 2, 4

Forstliche Pflanzgärten

Einjährige

Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Gemeine Quecke

Aufwandmenge: 2 - 3 l/ha

1, 2, 3

Forstliche Pflanzgärten

Mehrjährige

Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 4 - 10 l/ha

1, 2, 3

Auf und an National- und

Kantonsstrassen

Einjährige

Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Gemeine Quecke

Aufwandmenge: 2 - 3 l/ha

1, 2, 8

Auf und an National- und

Kantonsstrassen

Mehrjährige

Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 4 - 10 l/ha

1, 2, 8

Böschungen und Grünstreifen

entlang von Verkehrswegen

(gem. ChemRRV)

Einjährige

Dicotyledonen

(Unkräuter)

Einjährige

Monocotyledonen

(Ungräser)

Gemeine Quecke

Aufwandmenge: 2 - 3 l/ha

1, 2, 8

Böschungen und Grünstreifen

entlang von Verkehrswegen

(gem. ChemRRV)

Mehrjährige

Dicotyledonen

(Unkräuter)

Mehrjährige

Monocotyledonen

(Ungräser)

Aufwandmenge: 4 - 10 l/ha

1, 2, 8

A

Kultur

Schaderreger/

Wirkung

Dosierungshinweise

Auflagen

N Humusdeponie

Ackerkratzdistel

Stumpfblättriger

Ampfer (Blacken)

Konzentration: 5 - 10 %

Anwendung:

Einzelpflanzenbehandlung mit

Handspritzgeräten.

1, 2

Ö Grünfläche

Ackerkratzdistel

Stumpfblättriger

Ampfer (Blacken)

Konzentration: 5 - 10 %

Anwendung: Mit

Handspritzgeräten (ohne

Rückenspritze).

1, 2, 7, 9

Ö Grünfläche

Ackerkratzdistel

Stumpfblättriger

Ampfer (Blacken)

Konzentration: 0.5 - 1.5 %

Anwendung: Mit

Rückenspritze.

1, 2, 7, 9,

Ö Offene Ackerfläche

Ackerkratzdistel

Gemeine Quecke

Stumpfblättriger

Ampfer (Blacken)

Konzentration: 5 - 10 %

Anwendung: Mit

Handspritzgeräten (ohne

Rückenspritze).

1, 2, 9

Ö Offene Ackerfläche

Ackerkratzdistel

Gemeine Quecke

Stumpfblättriger

Ampfer (Blacken)

Konzentration: 0.5 - 1.5 %

Anwendung: Mit

Rückenspritze.

1, 2, 9, 10

Auflagen und Bemerkungen:

Keine Niederschläge während mindestens 6 Stunden nach der Behandlung.

Ansetzen der Spritzbrühe: Schutzhandschuhe tragen.

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

Herbizid in Kontakt kommen.

Behandlung bis spätestens 2 Wochen vor der Saat oder Pflanzung.

Die Aufwandmenge bezieht sich auf die effektiv zu behandelnde Fläche.

Behandlung der unbearbeiteten Zwischenreihen bei der Streifenfrässaat.

Beweidung oder Schnitt (Grünfutter oder Konservierung) frühestens 3 Wochen nach der

Behandlung. Ausnahme: Für nicht laktierende Tiere beträgt die Wartefrist 2 Wochen.

Gemäss Chemikalien-Risikoreduktions-Verordnung (ChemRRV): Nur Einzelpflanzenbehandlung

anderweitig nicht bekämpfbarer Problempflanzen.

Einzelpflanzenbehandlung gemäss Direktzahlungsverordnung (DZV).

10.Auf der Pakungsetikette ist die Empfehlung aufzuführen, dass vorzugsweise ein Handspritzgerät

verwendet werden soll.

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.

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

28-11-2018

Minister Bruno Bruins bereikt akkoord over openbare verlaging van prijzen voor geneesmiddelen tegen hepatitis C

Minister Bruno Bruins bereikt akkoord over openbare verlaging van prijzen voor geneesmiddelen tegen hepatitis C

Minister Bruno Bruins voor Medische Zorg heeft besloten acht nieuwe medicijnen tegen chronische hepatitis C te blijven vergoeden. Tot nu toe golden vertrouwelijke prijsafspraken voor deze middelen, maar die zijn vanaf 1 januari 2019 niet meer nodig. Twee leveranciers hebben gehoor gegeven aan een oproep van de minister voor een openbare prijsverlaging.

Netherlands - Ministerie van Volksgezondheid, Welzijn en Sport

22-11-2018

Foreign Product Alert: Black Ant King tablets, Gold Viagra 9800mg capsules, LIPRO Dietary capsules, Stree Overlord Strong tablets (pills), Vegetal Vigra capsules, ViaGro 500mg Male Enhancement capsules

Foreign Product Alert: Black Ant King tablets, Gold Viagra 9800mg capsules, LIPRO Dietary capsules, Stree Overlord Strong tablets (pills), Vegetal Vigra capsules, ViaGro 500mg Male Enhancement capsules

These foreign health products have been found by regulators in other countries to contain undeclared drug ingredients.

Health Canada

21-11-2018

Ulcergold ad us. vet., orale Paste

Ulcergold ad us. vet., orale Paste

● Die Neuzulassung erfolgte am 21.11.2018.

Institut für Veterinärpharmakologie und toxikologie

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

8-11-2018

Public Notification: Gold Max Blue contains hidden drug ingredient

Public Notification: Gold Max Blue contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Gold Max Blue, a product promoted and sold for sexual enhancement on various websites, including www.goldmaxblue.com, and possibly in some retail stores.

FDA - U.S. Food and Drug Administration

6-11-2018

Duncan Hines Classic White, Classic Butter Golden, Signature Confetti and Classic Yellow Cake Mixes Recalled Due to Potential Presence of Salmonella

Duncan Hines Classic White, Classic Butter Golden, Signature Confetti and Classic Yellow Cake Mixes Recalled Due to Potential Presence of Salmonella

Conagra Brands is collaborating with health officials in connection with a positive finding of Salmonella in a retail sample of Duncan Hines Classic White cake mix that may be linked to a Salmonella outbreak that is currently being investigated by CDC and FDA. While it has not been definitively concluded that this product is linked to the outbreak and the investigation is still ongoing, Conagra has decided to voluntarily recall the specific Duncan Hines variety identified (Classic White) and three other ...

FDA - U.S. Food and Drug Administration

18-10-2018

P. East Trading Corp. Issues Alert on Undeclared Sulfites In Fruits Du Sud Golden Seedless Raisins

P. East Trading Corp. Issues Alert on Undeclared Sulfites In Fruits Du Sud Golden Seedless Raisins

P. EAST TRADING CORP. of Bronx, NY is recalling Fruits Du Sud Golden Seedless Raisins (Lot No. FDS T499/18) 30 lbs Box, because they contain undeclared SULFITES. People who have a severe sensitivity to sulfites run the risk of serious or life-threatening reactions if they consume these products.

FDA - U.S. Food and Drug Administration

31-8-2018

Public Notification: PremierZen Gold 4000 contains hidden drug ingredient

Public Notification: PremierZen Gold 4000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use PremierZen Gold 4000, a product promoted for sexual enhancement. This product was identified during an examination of international mail shipments.

FDA - U.S. Food and Drug Administration

29-8-2018

Modification of the existing maximum residue levels for prohexadione in various oilseeds

Modification of the existing maximum residue levels for prohexadione in various oilseeds

Published on: Mon, 27 Aug 2018 00:00:00 +0200 In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant BASF SE submitted a request to the competent national authority in France to modify the existing maximum residue levels (MRL) for the active substance prohexadione in linseeds, poppy seeds, sunflower seeds, rape seeds, mustard seeds and gold of pleasure seeds. The data submitted in support of the request were found to be sufficient to derive MRL proposals for all oilseeds under consid...

Europe - EFSA - European Food Safety Authority Publications

14-8-2018

World Organix, LLC Issues Voluntary Nationwide Recall of Blissful Remedies Red Maeng Da 100% Mitragyna Speciosa, Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa, Blissful Remedies 4 Hour Chill Slow Motion Blend, Due to High Microbial Loads

World Organix, LLC Issues Voluntary Nationwide Recall of Blissful Remedies Red Maeng Da 100% Mitragyna Speciosa, Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa, Blissful Remedies 4 Hour Chill Slow Motion Blend, Due to High Microbial Loads

World Organix LLC, is voluntarily recalling lot: 112710 of Blissful Remedies Red Maeng Da 100% Mitragyna Speciosa capsules, Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa, Blissful Remedies 4 Hour Chill Slow Motion Blend to the consumer level. These products have been tested by the U.S. Food and Drug Administration (“FDA”) and found to be contaminated with High Microbial Loads. Additionally, this serves as a update to a previous press release posted on June 30th 2018, concerning Blissful...

FDA - U.S. Food and Drug Administration

31-7-2018

Public Notification: Gold Rhino 25000 contains hidden drug ingredient

Public Notification: Gold Rhino 25000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Gold Rhino 25000, a product promoted for sexual enhancement. This product was identified during an examination of international mail shipments.

FDA - U.S. Food and Drug Administration

24-7-2018

Pepperidge Farm® Announces Voluntary Recall of Four Varieties of Goldfish® Crackers

Pepperidge Farm® Announces Voluntary Recall of Four Varieties of Goldfish® Crackers

Pepperidge Farm has been notified by one of its ingredient suppliers that whey powder in a seasoning that is applied to four varieties of crackers has been the subject of a recall by the whey powder manufacturer due to the potential presence of Salmonella. Pepperidge Farm initiated an investigation and, out of an abundance of caution, is voluntarily recalling four varieties of Goldfish crackers. The products were distributed throughout the United States. No illnesses have been reported. ...

FDA - U.S. Food and Drug Administration

24-7-2018

Statement from FDA Commissioner Scott Gottlieb, M.D. on voluntary recalls of Ritz, Goldfish and other products issued out of an abundance of caution

Statement from FDA Commissioner Scott Gottlieb, M.D. on voluntary recalls of Ritz, Goldfish and other products issued out of an abundance of caution

The U.S. Food and Drug Administration is working with Mondelēz International, Inc., Pepperidge Farm Inc. and Flowers Foods, Inc. to initiate voluntarily recalls of certain products due to a potential risk that one of the ingredients may have been contaminated with Salmonella.

FDA - U.S. Food and Drug Administration

28-6-2018

Gold Maka tablets

Gold Maka tablets

Gold Maka tablets pose a serious risk to your health and should not be taken

Therapeutic Goods Administration - Australia

20-6-2018

Public Notification: Gold Viagra contains hidden drug ingredient

Public Notification: Gold Viagra contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Gold Viagra, a product promoted for sexual enhancement. This product was identified by FDA during an examination of international mail shipments.

FDA - U.S. Food and Drug Administration

19-6-2018

Golden Star Wholesale  Issues Allergy Alert on Undeclared Sulfites in Dried Apricots Sour

Golden Star Wholesale Issues Allergy Alert on Undeclared Sulfites in Dried Apricots Sour

Golden Star Wholesale of Troy, MI 48084 is recalling, AL Reef Dried Apricots Sour, because it may contain undeclared sulfites. People who have an allergy or severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.

FDA - U.S. Food and Drug Administration

23-5-2018

Golden International Corporation  Issues Public Safety Warning For Stolen Tilapia Because  of Possible Health Risk

Golden International Corporation Issues Public Safety Warning For Stolen Tilapia Because of Possible Health Risk

Golden International Corporation of Renton, WA is issuing a public safety notice for 405 cartons of stolen frozen tilapia, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection wi...

FDA - U.S. Food and Drug Administration

3-5-2018

Voluntary Recall of Certain Golden Flake, Good Health, UTZ and Weis Brand Tortilla Chips Because of Possible Milk Allergen

Voluntary Recall of Certain Golden Flake, Good Health, UTZ and Weis Brand Tortilla Chips Because of Possible Milk Allergen

Utz Quality Foods, LLC, is voluntarily recalling select expiration dates of some Golden Flake, Good Health, Utz and Weis Brand Tortilla Chip items due to potential contamination of undeclared milk allergen. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

FDA - U.S. Food and Drug Administration

28-4-2018

Tetra Goldfish GoldMed ad us. vet., Loesung

Tetra Goldfish GoldMed ad us. vet., Loesung

● Die Zulassung ist am 28.04.2018 erloschen.

Institut für Veterinärpharmakologie und toxikologie

17-4-2018

Gold Viagra 9800mg capsules

Gold Viagra 9800mg capsules

Safety advisory

Therapeutic Goods Administration - Australia

27-3-2018

Slim Trim Gold capsules

Slim Trim Gold capsules

Slim Trim Gold capsules pose a serious risk to your health and should not be taken

Therapeutic Goods Administration - Australia

26-11-2018


Withdrawn application: HopGuard Gold, purified semi-solid extract from Humulus lupulus L. containing approximately 48% of beta acids as potassium salts, Date of withdrawal: 12/04/2018, Initial authorisation

Withdrawn application: HopGuard Gold, purified semi-solid extract from Humulus lupulus L. containing approximately 48% of beta acids as potassium salts, Date of withdrawal: 12/04/2018, Initial authorisation

Withdrawn application: HopGuard Gold, purified semi-solid extract from Humulus lupulus L. containing approximately 48% of beta acids as potassium salts, Date of withdrawal: 12/04/2018, Initial authorisation

Europe - EMA - European Medicines Agency

26-11-2018

We aim to efficiently advance beneficial technology to patients, while solidifying FDA’s gold standard for safety. Our goal in focusing on older predicates is to drive sponsors to continually offer patients devices with the latest demonstrated improvement

We aim to efficiently advance beneficial technology to patients, while solidifying FDA’s gold standard for safety. Our goal in focusing on older predicates is to drive sponsors to continually offer patients devices with the latest demonstrated improvement

We aim to efficiently advance beneficial technology to patients, while solidifying FDA’s gold standard for safety. Our goal in focusing on older predicates is to drive sponsors to continually offer patients devices with the latest demonstrated improvements and advances in safety.

FDA - U.S. Food and Drug Administration

22-7-2018

Our aim: ensure that devices not only meet the gold standard for getting to market but continue to meet this standard as we get more data and learn more about their benefit-risk profile in real-world settings. These new approaches will also help advance b

Our aim: ensure that devices not only meet the gold standard for getting to market but continue to meet this standard as we get more data and learn more about their benefit-risk profile in real-world settings. These new approaches will also help advance b

Our aim: ensure that devices not only meet the gold standard for getting to market but continue to meet this standard as we get more data and learn more about their benefit-risk profile in real-world settings. These new approaches will also help advance beneficial innovation

FDA - U.S. Food and Drug Administration