Kerb Flo

Hauptinformation

  • Handelsname:
  • Kerb Flo
  • Darreichungsform:
  • SC Suspensionskonzentrat
  • 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:
  • Kerb Flo
    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:
  • D-5259
  • Letzte Änderung:
  • 15-11-2018

Packungsbeilage

Handelsbezeichnung: Kerb Flo (Parallelimport)

Pflanzenschutzmittelverzeichnis (Stand: 06.11.2018)

Produktkategorie:

Ausl. Bewilligungsinhaber:

Eidg. Zulassungsnummer:

Herbizid

Star Agro Analyse und Handels GmbH

D-5259

Stoff(e):

Gehalt:

Formulierungscode:

Wirkstoff: Propyzamide 35.09 % 400 g/l

SC Suspensionskonzentrat

Anwendungen

A

Kultur

Schaderreger/

Wirkung

Dosierungshinweise

Auflagen

B Freiland: Erdbeere

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 1.25 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

1, 2, 3

Freiland: Rote

Johannisbeere

Freiland: Schwarze

Johannisbeere

Freiland:

Stachelbeere

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 2.5 - 4 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

1, 2, 3, 4

Freiland: Rote

Johannisbeere

Freiland: Schwarze

Johannisbeere

Freiland:

Stachelbeere

Gemeine Quecke

Aufwandmenge: 5 - 6.25 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

2, 3, 4

Kernobst

Steinobst

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 2.5 - 4 l/ha

Anwendung: Winteranwendung (in der

Vegetationsruhe).

1, 2, 3

O Kernobst

Steinobst

Gemeine Quecke

Aufwandmenge: 5 - 6.25 l/ha

Anwendung: Winteranwendung (in der

2, 3

A

Kultur

Schaderreger/

Wirkung

Dosierungshinweise

Auflagen

Vegetationsruhe).

W Reben

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 2.5 - 4 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

1, 2, 3, 4

W Reben

Gemeine Quecke

Aufwandmenge: 5 - 6.25 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

2, 3, 4

Chicor

[Wurzelproduktion]

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 2.5 - 3.75 l/ha

Anwendung: Nach der Saat oder Pflanzung.

1, 3, 5, 6

G Estragon

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 3.75 l/ha

Wartefrist: 100 Tage

Anwendung: Vorauflauf. W

hrend der

Winterruhe.

1, 3, 6, 7

G Rhabarber

Einj

hrige

Dicotyledonen (Unkr

uter)

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 3.75 l/ha

Anwendung: Oktober - Dezember

1, 3, 6, 8,

mische Kamille

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 3.75 l/ha

Wartefrist: 100 Tage

Anwendung: Anwendung nach der

Pflanzung und nach dem Anwachsen der

Kultur im Herbst oder Anwendung im

Winter w

hrend der Vegetationsruhe oder

Anwendung von M

rz bis Mai auf die

bestehende Kultur.

1, 3, 5, 6,

G Freiland: Salate

(Asteraceae)

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

Aufwandmenge: 2.5 - 3.75 l/ha

Anwendung: Nach der Saat oder Pflanzung.

1, 3, 5

A

Kultur

Schaderreger/

Wirkung

Dosierungshinweise

Auflagen

(Ungr

ser)

G Freiland: Schnittlauch

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 2 l/ha

Wartefrist: 45 Tage

1, 3, 6, 10

Raps

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 1.25 - 1.875 l/ha

Anwendung: Nachauflauf Herbst: Stadium

14-16 (BBCH).

1, 3, 11

ume und Str

ucher (ausserhalb

Forst)

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 2.5 - 4 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

1, 2, 3, 4

ume und Str

ucher (ausserhalb

Forst)

Gemeine Quecke

Aufwandmenge: 5 - 6.25 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

2, 3, 4

Auflagen und Bemerkungen:

Keine Wirkung auf Klebern und Korbbl

tler wie Franzosenkraut, Kamille und Kreuzkraut.

Auf schnee- und eisfreien Boden.

Ansetzen der Spritzbr

he: Schutzhandschuhe + Schutzanzug 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.

Anwendung fr

hestens 6 Monate nach Pflanzung.

Bei geringen Niederschl

gen und in trockenen Gebieten muss das Produkt nach der Applikation

eingeregnet werden.

Bewilligt als geringf

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

Anwendung nur in Kulturen zur Produktion von

therischen Ölen f

r die Kosmetikindustrie.

Keine Behandlung im Pflanzjahr.

Behandlung nur w

hrend der vollst

ndigen Winterruhe der Kultur.

10.Behandlung w

hrend der Vegetationsruhe: nach dem Schnitt vor dem erneuten Austrieb.

11.Nach Umbruch von Raps wegen Auswinterung d

rfen keine Getreidearten angebaut werden.

Kartoffeln, R

ben, Erbsen, Bohnen, Sommerraps und Mais sind f

r den Nachbau geeignet.

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.

1-11-2018

Pest categorisation of Conotrachelus nenuphar

Pest categorisation of Conotrachelus nenuphar

Published on: Wed, 31 Oct 2018 00:00:00 +0100 The EFSA Panel on Plant Health performed a pest categorisation of Conotrachelus nenuphar (Herbst) (Coleoptera: Curculionidae), for the EU. C. nenuphar is a well‐defined species, recognised as a serious pest of stone and pome fruit in the USA and Canada where it also feeds on a range of other hosts including soft fruit (e.g. Ribes,Fragaria) and wild plants (e.g. Crataegus). Adults, which are not good flyers, feed on tender twigs, flower buds and leaves. Femal...

Europe - EFSA - European Food Safety Authority Publications

1-11-2018

Pest categorisation of Acrobasis pirivorella

Pest categorisation of Acrobasis pirivorella

Published on: Wed, 31 Oct 2018 00:00:00 +0100 The European Commission requested EFSA to conduct a pest categorisation of Acrobasis pirivorella (Lepidoptera: Pyralidae), a monophagous moth whose larvae exclusively feed on developing buds, flowers, and fruits of cultivated and wild Pyrus spp. A. pirivorella is a species with reliable methods available for identification. A. pirivorellaoccurs in north‐east Asia only, causing significant damage in cultivated pears. It is regulated in the EU by Council Direc...

Europe - EFSA - European Food Safety Authority Publications

30-10-2018

Pest categorisation of Aleurocanthus spp.

Pest categorisation of Aleurocanthus spp.

Published on: Mon, 29 Oct 2018 00:00:00 +0100 The Panel on Plant Health performed a pest categorisation of Aleurocanthus spp., a well‐defined insect genus of the whitefly family Aleyrodidae (Arthropoda: Hemiptera). Difficulties within the taxonomy of the genus give doubt about the ability to accurately identify some members to species level. Nevertheless, the genus is thought to currently include about ninety species mainly reported from tropical and subtropical areas. The genus is listed in Council Dir...

Europe - EFSA - European Food Safety Authority Publications

25-10-2018

i play., inc. recalls Flower Rattle

i play., inc. recalls Flower Rattle

Pieces of the rattle can detach, posing a choking hazard to infants.

Health Canada

22-10-2018

Promise Pharmacy Issues Voluntary Nationwide Recall of Prednisolone and Gatifloxacin Ophthalmic Solution 1%/0.5% Sterile Due to Small Particulate Floating in the Solution

Promise Pharmacy Issues Voluntary Nationwide Recall of Prednisolone and Gatifloxacin Ophthalmic Solution 1%/0.5% Sterile Due to Small Particulate Floating in the Solution

Promise Pharmacy is voluntarily recalling one lot of Prednisolone and Gatifloxacin Ophthalmic Solution 1%/0.5% sterile, 3ml vials, to the patient consumer level. The product has been found to have unidentified small particulate floating in the solution.

FDA - U.S. Food and Drug Administration

12-10-2018

Voluntary Recall of Limited Amounts of Nuts & Vanilla Protein Plant Shake

Voluntary Recall of Limited Amounts of Nuts & Vanilla Protein Plant Shake

Forager Project is recalling three dates of Nuts and Vanilla – Organic Plant Protein Shake because the product contains almond flour which is not declared on the label.

FDA - U.S. Food and Drug Administration

22-9-2018

Risk assessment of new sequencing information on genetically modified carnation FLO‐40689‐6

Risk assessment of new sequencing information on genetically modified carnation FLO‐40689‐6

Published on: Fri, 21 Sep 2018 00:00:00 +0200 The GMO Panel has previously assessed genetically modified (GM) carnation FLO‐40689‐6 and concluded that there is no scientific reason to consider that the import, distribution and retailing in the EU of carnation FLO‐40689‐6 cut flowers for ornamental use will cause any adverse effects on human health or the environment. On 27 October 2017, the European Commission requested EFSA to analyse new nucleic acid sequencing data and updated bioinformatics data for...

Europe - EFSA - European Food Safety Authority Publications

29-8-2018

Scientific Opinion about the Guidance of the Chemical Regulation Directorate (UK) on how aged sorption studies for pesticides should be conducted, analysed and used in regulatory assessments

Scientific Opinion about the Guidance of the Chemical Regulation Directorate (UK) on how aged sorption studies for pesticides should be conducted, analysed and used in regulatory assessments

Published on: Mon, 27 Aug 2018 00:00:00 +0200 The EFSA Panel on Plant Protection Products and their Residues reviewed the guidance on how aged sorption studies for pesticides should be conducted, analysed and used in regulatory assessment. The inclusion of aged sorption is a higher tier in the groundwater leaching assessment. The Panel based its review on a test with three substances taken from a data set provided by the European Crop Protection Association. Particular points of attention were the quali...

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

7-8-2018

Voluntary Recall Notice of El Guapo Jamaica Hibiscus Flower Pouches Due to Unlabeled Peanut Allergen

Voluntary Recall Notice of El Guapo Jamaica Hibiscus Flower Pouches Due to Unlabeled Peanut Allergen

Mojave Foods Corporation is initiating a voluntary recall of four sizes of El Guapo Jamaica Hibiscus Flower packages in flexible packaging due to an unlabeled peanut allergen

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

23-7-2018

Flowers Foods Issues Voluntary Recall on Mrs. Freshley’s and Other Brands of Swiss Rolls and Captain John Derst’s Old Fashioned Bread

Flowers Foods Issues Voluntary Recall on Mrs. Freshley’s and Other Brands of Swiss Rolls and Captain John Derst’s Old Fashioned Bread

As a precautionary measure, Flowers Foods, Inc. (NYSE: FLO) is voluntarily recalling Swiss Rolls sold under the brand names Mrs. Freshley’s, Food Lion, H-E-B, Baker’s Treat, Market Square, and Great Value, distributed nationwide, and Captain John Derst’s Old Fashioned Bread distributed in Alabama, Florida, Georgia, North Carolina, and South Carolina, due to the potential presence of Salmonella in an ingredient, whey powder. The ingredient recall was initiated by a third-party whey powder manufacturer and...

FDA - U.S. Food and Drug Administration

13-7-2018

Water Pik, Inc. Recalls Sonic-Fusion® Flossing Toothbrush Product for Possible Health Risk

Water Pik, Inc. Recalls Sonic-Fusion® Flossing Toothbrush Product for Possible Health Risk

Water Pik, Inc. is voluntarily recalling its Sonic-Fusion® flossing toothbrush because the charging base may overheat with localized melting and sparking, possibly causing fire, shock or burns. Water Pik, Inc. has received consumer reports of product malfunctioning in the U.S. The recall is applicable only to Sonic-Fusion® products. All other Waterpik® brand flossers and toothbrushes are not affected.

FDA - U.S. Food and Drug Administration

2-7-2018

May Flower International Inc. Issues a Allergy Alert on Undeclared Milk Allergens in “3+2 Soda Crackers”

May Flower International Inc. Issues a Allergy Alert on Undeclared Milk Allergens in “3+2 Soda Crackers”

May Flower International Inc. of 5672 49th Place, Maspeth, NY, is recalling its 4.4 ounce packages of “3+2 Soda Crackers” because they may contain undeclared milk allergens. Consumers who are allergic to milk allergens may run the risk of serious or life threatening allergic reactions if they consume this product.

FDA - U.S. Food and Drug Administration

1-7-2018

Allergy Alert Issued in Midwest Whole Foods Market Stores for Undeclared Soy in Oatmeal Raisin Cookies

Allergy Alert Issued in Midwest Whole Foods Market Stores for Undeclared Soy in Oatmeal Raisin Cookies

Whole Foods Market is voluntarily recalling Whole Foods Market brand oatmeal raisin cookies from stores in eight states because the products contained soy flour that was not listed on the product label. People who have an allergy or severe sensitivity to soy run the risk of serious or life-threatening allergic reaction if they consume these products.

FDA - U.S. Food and Drug Administration

23-6-2018

Dringende Sicherheitsinformation zu Mentype® MycoDermQS Lateral Flow von Biotype Diagnostic GmbH

Dringende Sicherheitsinformation zu Mentype® MycoDermQS Lateral Flow von Biotype Diagnostic GmbH

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

Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

15-6-2018

Compounded Products Containing Triamcinolone-Moxifloxacin by Guardian Pharmacy Services (Dallas, Texas): Alert to Health Professionals - Adverse Events Reported After Receiving Eye Injections

Compounded Products Containing Triamcinolone-Moxifloxacin by Guardian Pharmacy Services (Dallas, Texas): Alert to Health Professionals - Adverse Events Reported After Receiving Eye Injections

At least 43 patient reported adverse event after receiving eye injections of Guardian’s Pharmacy Services compounded triamcinolone-moxifloxacin product during cataract surgery. The patients reportedly experienced various symptoms, including vision impairment, poor night vision, loss of color perception, and significant reductions in best-corrected visual acuity and visual fields. FDA identified multiple substances in Guardian’s product, including poloxamer 407 and poloxamer 407 degradants. FDA prepared i...

FDA - U.S. Food and Drug Administration

5-6-2018

Dringende Sicherheitsinformation zu Biograph mCT systems, Biograph mCT Flow systems von Siemens Medical Solutions USA, Inc. Molecular Imaging

Dringende Sicherheitsinformation zu Biograph mCT systems, Biograph mCT Flow systems von Siemens Medical Solutions USA, Inc. Molecular Imaging

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

Deutschland - BfArM - Bundesinstitut für Arzneimittel und Medizinprodukte

31-5-2018

Abbott Implements Corrective Action for Heartmate 3 Heart Pump

Abbott Implements Corrective Action for Heartmate 3 Heart Pump

Abbott is communicating to physicians about a field corrective action related to the HeartMate 3™ Left Ventricular Assist Device (LVAD). Abbott notified physicians and global regulatory bodies on April 5, 2018, that outflow graft twisting could occur post-implant in the HeartMate 3 LVAD, resulting in a persistent low flow alarm that may signal a potential safety risk to patients, such as low blood flow or clotting.

FDA - U.S. Food and Drug Administration

25-5-2018

Urgent Medical Device Recall: Sam XT Extremity Tourniquet

Urgent Medical Device Recall: Sam XT Extremity Tourniquet

SAM Medical today announced it is conducting a voluntary international recall of all unused SAM XT Extremity Tourniquets (SAM XT). The company initiated the recall after internal testing indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human patient to stop arterial blood flow. To date, there have been no reports of adverse health consequences received. This recall is being made with the knowledge of the Food and Drug A...

FDA - U.S. Food and Drug Administration

22-5-2018

HeartMate 3™ Left Ventricular Assist System: Class I Recall - Due to Potential Malfunction that may Lead to Graft Occlusion

HeartMate 3™ Left Ventricular Assist System: Class I Recall - Due to Potential Malfunction that may Lead to Graft Occlusion

The class I recall is due to a malfunction in the device’s outflow graft assembly that may cause the outflow graft to twist and close up (occlusion) over time. Occlusion of the outflow graft can reduce or stop pump flow and set off a persistent low flow alarm in the system. A reduction in pump can lead to serious adverse events such as blood clots and death.

FDA - U.S. Food and Drug Administration

9-1-2018

Adding Folic Acid to Corn Masa Flour May Prevent Birth Defects

Adding Folic Acid to Corn Masa Flour May Prevent Birth Defects

When consumed by women before and during pregnancy, folic acid, a B vitamin, may help prevent neural tube defects (NTDs).

FDA - U.S. Food and Drug Administration

14-11-2018

Ofloxacin-Ophtal 3 mg/g Augensalbe

Rote - Liste

14-11-2018

Floxal® 3 mg/ml Augentropfen

Rote - Liste

14-11-2018

Floxal® 3 mg/g Augensalbe

Rote - Liste

24-9-2018

If you use a #MedicalDevice affected by a power outage caused by #HurricaneFlorence, check out the #FDA’s tips for using a generator to restore power to your device:  https://go.usa.gov/xPjau pic.twitter.com/z8SW2mlb86

If you use a #MedicalDevice affected by a power outage caused by #HurricaneFlorence, check out the #FDA’s tips for using a generator to restore power to your device: https://go.usa.gov/xPjau pic.twitter.com/z8SW2mlb86

If you use a #MedicalDevice affected by a power outage caused by #HurricaneFlorence, check out the #FDA’s tips for using a generator to restore power to your device: https://go.usa.gov/xPjau  pic.twitter.com/z8SW2mlb86

FDA - U.S. Food and Drug Administration

11-6-2018

Quinsair (Chiesi Farmaceutici S.p.A.)

Quinsair (Chiesi Farmaceutici S.p.A.)

Quinsair (Active substance: levofloxacin) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3756 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2789/T/16

Europe -DG Health and Food Safety