Ridomil Gold SL

Hauptinformation

  • Handelsname:
  • Ridomil Gold SL
  • 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:
  • Ridomil Gold SL
    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-5252
  • Letzte Änderung:
  • 15-11-2018

Packungsbeilage

Handelsbezeichnung: Ridomil Gold SL

(Parallelimport)

Pflanzenschutzmittelverzeichnis (Stand: 06.11.2018)

Bewilligung beendet: Ausverkaufsfrist: 31.05.2018, Aufbrauchsfrist: 31.05.2019

Produktkategorie:

Ausl. Bewilligungsinhaber:

Eidg. Zulassungsnummer:

Fungizid

Star Agro Analyse und Handels GmbH

D-5252

Stoff(e):

Gehalt:

Formulierungscode:

Wirkstoff: Metalaxyl-M 43.9 % 465 g/l

SL Wasserl

sliches

Konzentrat

Anwendungen

A

Kultur

Schaderreger/Wirkung

Dosierungshinweise

Auflagen

Chicor

Phytophthora cryptogea

Aufwandmenge: 10 ml/hl

Wartefrist: 3 Woche(n)

Anwendung: Tauchbehandlung der

Wurzeln. Zu Beginn der Treiberei.

1, 2, 4

Chicor

Phytophthora cryptogea

Aufwandmenge: 4 ml/t

Wartefrist: 3 Woche(n)

Anwendung: Zu Beginn der

Treiberei. Spritzbehandlung der

Wurzeln.

1, 2, 3

G Karotten

Pythium spp.

Aufwandmenge: 0.5 l/ha

Anwendung: Stadium 11-14

(BBCH). Spritzapplikation.

5, 6

chenkr

uter

Falsche Mehltaupilze

der K

chenkr

uter

Aufwandmenge: 0.2 - 0.22 l/ha

Wartefrist: 3 Woche(n)

Anwendung: Spritzapplikation.

chshaus: B

und Str

ucher

(ausserhalb Forst)

chshaus:

Blumenkulturen und Gr

npflanzen

Falsche Mehltaupilze

der Zierpflanzen

Phytophthora spp.

Pythium spp.

Konzentration: 0.02 %

Anwendung: Spritzapplikation.

7, 8, 10

A

Kultur

Schaderreger/Wirkung

Dosierungshinweise

Auflagen

chshaus: B

und Str

ucher

(ausserhalb Forst)

chshaus:

Blumenkulturen und Gr

npflanzen

Falsche Mehltaupilze

der Zierpflanzen

Phytophthora spp.

Pythium spp.

Aufwandmenge: 5 l/ha

Anwendung: Giessbehandlung.

9, 11, 12

chshaus: B

und Str

ucher

(ausserhalb Forst)

chshaus:

Blumenkulturen und Gr

npflanzen

Falsche Mehltaupilze

der Zierpflanzen

Phytophthora spp.

Pythium spp.

Aufwandmenge: 25 ml/m3

Pflanzenerde

Anwendung: Behandlung der

Pflanzenerde.

Auflagen und Bemerkungen:

Maximal 1 Behandlung.

Bewilligt als geringf

gige Verwendung nach Art. 35 PSMV (minor use).

Ansetzen der Spritzbr

he: Schutzhandschuhe + Schutzbrille oder Visier tragen. Ausbringen der

Spritzbr

he: Schutzhandschuhe tragen.

Ansetzen der Br

he: Schutzhandschuhe + Schutzbrille oder Visier tragen. Behandlung:

Schutzhandschuhe tragen.

Maximal 1 Behandlung pro Kultur.

Ansetzen der Spritzbr

he: Schutzhandschuhe + Schutzbrille oder Visier tragen. Ausbringen der

Spritzbr

he: Schutzhandschuhe + Schutzanzug tragen. Technische Schutzvorrichtungen w

hrend des Ausbringens (z.B. geschlossene Traktorkabine) k

nnen die vorgeschriebene pers

nliche Schutzausr

stung ersetzen, wenn gew

hrleistet ist, dass sie einen vergleichbaren oder h

heren Schutz bieten.

Ansetzen der Spritzbr

he: Schutzhandschuhe + Schutzbrille oder Visier tragen.

Maximal 3 Behandlungen pro Parzelle und Jahr.

Maximal 2 Behandlungen pro Kultur.

10.Nachfolgearbeiten in behandelten Kulturen: bis 48 Stunden nach Ausbringung des Mittels

Schutzhandschuhe + Schutzanzug tragen.

11.Erste Behandlung nach der Pflanzung, zweite Behandlung 3 Wochen sp

ter.

12.Ansetzen der Giessbr

he: Schutzhandschuhe + Schutzbrille oder Visier tragen.

13.Ansetzen der Br

he: Schutzhandschuhe + Schutzbrille oder Visier tragen.

Gefahrenkennzeichnungen:

Es gilt die Einstufung und Kennzeichnung der ausl

ndischen Originaletikette..

tzliche Schweizerische Gefahrenkennzeichnungen:

SP 1 Mittel und/oder dessen Beh

lter nicht in Gew

sser gelangen lassen.

Im Zweifelsfall gelten einzig die Originaldokumente der Zulassung. Die Erw

hnung eines Produktes,

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

Verkauf befindet.

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

14-9-2018

Hepar-SL® 640 mg

Rote - Liste

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

29-5-2018

EU/3/18/2016 (Abeona Therapeutics Europe SL)

EU/3/18/2016 (Abeona Therapeutics Europe SL)

EU/3/18/2016 (Active substance: Adeno-associated viral vector serotype 9 containing the human CLN1 gene) - Orphan designation - Commission Decision (2018)3383 of Tue, 29 May 2018 European Medicines Agency (EMA) procedure number: EMA/OD/013/18

Europe -DG Health and Food Safety