COPPER OXYCHLORIDE

Main information

  • Trade name:
  • AMGROW CHEMSPRAY DISEASE CONTROL COPPER OXYCHLORIDE FUNGICIDE
  • Pharmaceutical form:
  • Wettable
  • Units in package:
  • 200g
  • Class:
  • AgChem
  • Medicine domain:
  • Equipment
  • Medicine type:
  • Agrochemical
  • Manufactured by:
  • AMGROW

Documents

Localization

  • Available in:
  • AMGROW CHEMSPRAY DISEASE CONTROL COPPER OXYCHLORIDE FUNGICIDE
    Australia
  • Language:
  • English

Therapeutic information

  • Therapeutic group:
  • APPLE | AVOCADO | BRASSICA VEGETABLES | CAPSICUM OR PEPPER | CARROT | CELERY | CITRUS FRUIT OR TREE | CUCURBIT | FRENCH BEAN | G
  • Therapeutic area:
  • Group M1 Fungicide
  • Therapeutic indications:
  • ANGULAR LEAF SPOT - P. GRISEOLA | ANTHRACNOSE | ASCOCHYTA BLIGHT | BACTERIAL BLIGHT | BACTERIAL BROWN SPOT | BACTERIAL LEAF SPOT | BACTERIAL SPECK | BACTERIAL SPOT - XANTHOMONAS VESICATORIA | BLACK SPOT - COLLETOTRICHUM ACUTATUM | BLACK SPOT OR SPECKLED BLOTCH ON CITRUS | BLACK SPOT/SCAB IN APPLE/PEAR | BLOSSOM BLIGHT - MONILINIA LAXA | BROWN SPOT ON PASSIONFRUIT | CITRUS MELANOSE | COMMON BLIGHT | DOWNY MILDEW | EARLY BLIGHT | EARLY BLIGHT (TARGET SPOT) | FRECKLE OR SCAB ON STONE FRUIT | FUNGUS | LATE BLIGHT OR IRISH BLIGHT | LEAF CURL | LEAF SPOT - ALTERNARIA CERCOSPORA | PEPPERY LEAF SPOT | RING SPOT | SEPTORIA LEAF SPOT - SEPTORIA APIICOLA | SEPTORIA SPOT | SEPTORIA SPOT ON PASSIONFRUIT | SHOTHOLE | STONE FRUIT RUST | ANTHRACNOSE | APPLE SCAB | BACTERIAL BLIGHT | BROWN ROT | CELERY LEAF SPOT | CERCOSPORA | CLASTEROSPORIUM | FRECKLE (SCAB) | FRUCTICOLA | FUNGAL LEAF SPOTS | FUNGI | FUNGUS DISEASES | IRISH BLIGHT | LATE BLIGHT | LEAF BLIGHT - S. APIICOLA | LEAF SPOT DISEASES | LEAF SPOTS | LEPTOSPHAERULINA
  • Product summary:
  • For the control of certain fungal diseases of fruit trees, vegetables and ornamentals in the home garden.

Other information

Status

  • Source:
  • Australian Pesticides and Veterinary Medicines Authority (APVMA)
  • Authorization status:
  • Registered and available
  • Authorization number:
  • 30306/52939
  • Authorization date:
  • 13-04-2011
  • Last update:
  • 15-06-2017

Patient Information leaflet: composition, indications, side effects, dosage, interactions, adverse reactions, pregnancy, lactation

Main panel bottle

POISON

KEEP OUT OF REACH OF CHILDREN

READ SAFETY DIRECTIONS

Amgrow

Chemspray

DISEASE CONTROL

COPPER OXYCHLORIDE

Fungicide

ACTIVE CONSTITUENT:

500 g/kg COPPER (Cu) present as COPPER OXYCHLORIDE

For the control of certain fungal diseases of fruit trees, vegetables and

ornamentals in the home garden.

Before using product, read directions on outer pack.

Sale of this bottle except in outer pack is illegal.

NET CONTENTS 200 g

Amgrow Chemspray Disease Control Copper Oxychloride Fungicide label

21/03/11

30306/52939 200 g bottle and carton

page 1 of 6

RLP

APPROVED

Info

pest

Verified

Ancillary panel bottle

STORAGE & DISPOSAL:

Store in the closed, original container in a cool, dry place out

of the reach of children. Do not store in direct sunlight. Dispose of empty container by

wrapping in paper, placing in plastic bag and putting in garbage.

SAFETY DIRECTIONS: Harmful if swallowed. May irritate the eyes and skin. Avoid

contact with eyes and skin. Wash hands after use.

FIRST AID:

If poisoning occurs, contact a Doctor or Poisons Information Centre. Phone

Australia 131126.

NOTE: this product is sold by weight not volume. The contents may settle during transit.

APVMA Approval No. 30306/52939

Amgrow Pty Ltd

A.B.N. 81 100 684 786

82 Christensen Road, Stapylton Qld 4207

Customer Service Number

1800 063 619

www.amgrow.com.au

Batch number:

Date of Manufacture:

BAR CODE

Amgrow Chemspray Disease Control Copper Oxychloride Fungicide label

21/03/11

30306/52939 200 g bottle and carton

page 2 of 6

Main panel carton

POISON

KEEP OUT OF REACH OF CHILDREN

READ SAFETY DIRECTIONS

Amgrow

Chemspray

DISEASE CONTROL

COPPER OXYCHLORIDE

Fungicide

ACTIVE CONSTITUENT:

500 g/kg COPPER (Cu) present as COPPER OXYCHLORIDE

For the control of certain fungal diseases of fruit trees, vegetables and

ornamentals in the home garden.

The bottle must not be sold separately.

Do not destroy box while product still remains.

NET CONTENTS 200 g

Amgrow Chemspray Disease Control Copper Oxychloride Fungicide label

21/03/11

30306/52939 200 g bottle and carton

page 3 of 6

Ancillary panel 1 carton

HOW TO USE:

Crop

Disease

State

Rate

How To Apply

Apples

Pears

Black Spot

(Scab)

All States

5g per 2 litres

of water + 5mL

white oil

Apply at green tip.

Avocados

Anthracnose

Qld, NSW,

NT, SA, Vic

only

5g per 2 litres

of water

Apply from flowering to harvest at 28-day

intervals.

Common

Blight

SA, Tas, Vic,

WA only

Apply every 10-14 days when disease first

appears.

Beans

(French)

Bacterial

Brown Spot

All States

5g per 2 litres

of water

Apply the first spray within 3 weeks of emergence

and repeat every 10-14 days.

Brassicas

(cabbage,

broccoli etc)

Black Spot,

Peppery leaf

spot, Ring

Spot, Downy

Mildew

All States

5g per 2 litres

of water

Apply every 14 days.

Capsicums

Bacterial Spot

All States

5g per 2 litres

of water

Apply every 10-14 days.

Carrots

Leaf Spot

All States

5g per 2 litres

of water

Apply at 7-14 day intervals.

Septoria Spot

All States

Celery

Early Blight

NSW, Vic,

SA, WA, NT

only

5g per 2 litres

of water

Apply at 7-14 day intervals.

Citrus

Black Spot

Melanose

NSW, SA,

Vic, WA only

7g per 4 litres

of water + 6mL

of white oil

Apply at 50-80% petal fall and again after 6 –12

weeks if necessary.

Cucurbits

(Cucumbers,

Melons etc)

Angular Leaf

Spot, Bacterial

Leaf Spot

All States

5g per 2 litres

of water

Apply at 10-14 day intervals.

Grape vines

Downy Mildew

NSW, Qld,

SA, Tas, Vic,

WA only

5g per 2 litres

of water

Commence when shoots are approx. 20cm long

and apply at 14-21 day intervals. Do not apply

during flowering.

Lettuce

Downy Mildew

All States

5g per 2 litres

of water

Spray when disease first appears or as a

preventative and repeat every 10 days if

necessary.

Onions

Downy Mildew

All States

5g per 2 litres

of water

Apply at 10 day intervals.

Ornamentals

(Flowers and

Shrubs)

Fungal Leaf

Spots, Downy

Mildew

All States

3g per litre of

water

Apply when disease first appears.

Repeat at 7-14 day intervals.

Qld only

2g per litre of

water

Passionfruit

Brown Spot,

Septoria Spot

NSW, NT,

Vic, SA, Tas,

WA only

3g to 4g per

litre of water

Apply every 7-14 days.

Peas

Ascochyta

Blight,

Bacterial Blight

All States

5g per 2 litres

of water

Apply at 7-14 day intervals.

Potatoes

Target Spot

(Early Blight),

Late (or Irish)

Blight

All States

5g per 2 litres

of water

Apply at 7-14 day intervals.

Silver Beet

Spinach

Downy Mildew

All States

5g per 2 litres

of water

Apply at 10-14 day intervals.

Amgrow Chemspray Disease Control Copper Oxychloride Fungicide label

21/03/11

30306/52939 200 g bottle and carton

page 4 of 6

Blossom

Blight, Freckle,

Rust

Apply at budswell.

Stone Fruit

(eg peaches,

nectarines)

Leaf Curl, Shot

Hole

NSW, Vic,

Tas, SA, WA

only

4g per litre of

water

Apply at budswell. For shot hole apply again at

leaf fall..

Bacterial Spot

Bacterial

Speck

Target

Spot/Early

Blight

Tomatoes

Septoria Leaf

Spot, Irish &

Late Blight

All States

5g per 2 litres

of water

Apply at 7-14 day intervals.

NOT TO BE USED FOR ANY PURPOSE, OR IN ANY MANNER, CONTRARY TO

THIS LABEL UNLESS AUTHORISED.

DO NOT PICK FRUIT AND VEGETABLES FOR 1 DAY AFTER SPRAYING.

Amgrow Chemspray Disease Control Copper Oxychloride Fungicide label

21/03/11

30306/52939 200 g bottle and carton

page 5 of 6

Ancillary panel 2 carton

HOW TO PREPARE

Add the required quantity of product to water and stir thoroughly. Mix required oil with

equal volume of water prior to adding to spray mixture. Carefully follow

recommended rates and timing for application.

CAUTION: DO NOT allow chemical containers or spray to get into drains, sewers,

streams or ponds.

STORAGE & DISPOSAL:

Store in the closed, original container in a cool, dry place out

of the reach of children. Do not store in direct sunlight. Dispose of empty container by

wrapping in paper, placing in plastic bag and putting in garbage.

SAFETY DIRECTIONS: Harmful if swallowed. May irritate the eyes and skin. Avoid

contact with eyes and skin. Wash hands after use.

FIRST AID:

If poisoning occurs, contact a Doctor or Poisons Information Centre. Phone

Australia 131126.

NOTE: this product is sold by weight not volume. The contents may settle during transit.

APVMA Approval No. 30306/52939

Amgrow Pty Ltd

A.B.N. 81 100 684 786

82 Christensen Road, Stapylton Qld 4207

Customer Service Number

1800 063 619

www.amgrow.com.au

Batch number:

Date of Manufacture:

BAR CODE

Amgrow Chemspray Disease Control Copper Oxychloride Fungicide label

21/03/11

30306/52939 200 g bottle and carton

page 6 of 6

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Safety evaluation of the food enzyme glucan 1,4‐α‐glucosidase from a genetically modified Aspergillus niger (strain NZYM‐BW)

Safety evaluation of the food enzyme glucan 1,4‐α‐glucosidase from a genetically modified Aspergillus niger (strain NZYM‐BW)

Published on: Wed, 31 Oct 2018 00:00:00 +0100 The food enzyme glucan 1,4‐α‐glucosidase (EC 3.2.1.3) is produced with the genetically modified Aspergillus niger strain NZYM‐BW by Novozymes A/S. The genetic modifications do not give rise to safety concerns. The food enzyme is free from viable cells of the production organism and recombinant DNA. The glucan 1,4‐α‐glucosidase food enzyme is intended to be used in distilled alcohol production and starch processing for the production of glucose syrups. Residu...

Europe - EFSA - European Food Safety Authority Publications

1-11-2018

Safety of the food enzyme glucoamylase from a genetically modified Aspergillus niger (strain NZYM‐BF)

Safety of the food enzyme glucoamylase from a genetically modified Aspergillus niger (strain NZYM‐BF)

Published on: Wed, 31 Oct 2018 00:00:00 +0100 The food enzyme glucoamylase (glucan 1,4‐α‐glucosidase; EC 3.2.1.3) is produced with the genetically modified strain of Aspergillus niger by Novozymes A/S. The genetic modifications do not give rise to safety concerns. The food enzyme is free from viable cells of the production organism and recombinant DNA. This glucoamylase is intended to be used in brewing processes and in starch processing for glucose syrups production. Residual amounts of total organic s...

Europe - EFSA - European Food Safety Authority Publications

1-11-2018

Safety evaluation of the food enzyme α‐amylase from a genetically modified Aspergillus niger (strain NZYM‐MC)

Safety evaluation of the food enzyme α‐amylase from a genetically modified Aspergillus niger (strain NZYM‐MC)

Published on: Wed, 31 Oct 2018 00:00:00 +0100 The food enzyme alpha‐amylase (4‐α‐d‐glucan glucanohydrolase; EC 3.2.1.1) is produced with the genetically modified strain of Aspergillus niger by Novozymes A/S. The genetic modifications do not give rise to safety concerns. The food enzyme is free from viable cells of the production organism and recombinant DNA. This α‐amylase is intended to be used in starch processing for glucose syrups production, beverage alcohol (distilling) processes and baking proces...

Europe - EFSA - European Food Safety Authority Publications

31-10-2018

Safety and efficacy of a super critical carbon dioxide extract of Humulus lupulus L. flos when used as a feed flavouring for all animal species

Safety and efficacy of a super critical carbon dioxide extract of Humulus lupulus L. flos when used as a feed flavouring for all animal species

Published on: Tue, 30 Oct 2018 00:00:00 +0100 Following a request from the European Commission, the EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety and efficacy of a super critical carbon dioxide extract of Humulus lupulus L. flos (hop strobiles) when used as a sensory feed additive for all animal species. The additive is specified to containing 40% beta acids and less than 0.2% alpha acids. Known substances of conce...

Europe - EFSA - European Food Safety Authority Publications

31-10-2018

Efficacy of Bergazym® P100 (endo‐1,4‐β‐xylanase) as a feed additive for chickens for fattening and weaned piglets

Efficacy of Bergazym® P100 (endo‐1,4‐β‐xylanase) as a feed additive for chickens for fattening and weaned piglets

Published on: Tue, 30 Oct 2018 00:00:00 +0100 The product Bergazym® P100 contains a xylanase which is produced by a non‐genetically modified strain of Trichoderma reesei. The additive is available in a coated granular form and it is intended to be used as a zootechnical additive (functional group: digestibility enhancers) for chickens for fattening, and weaned piglets at the dose of 1,500 EPU/kg feed. The production strain and the additive were fully characterised in a previous assessment of the Panel o...

Europe - EFSA - European Food Safety Authority Publications

31-10-2018

Safety and efficacy of Lactobacillus hilgardii CNCM I‐4785 and Lactobacillus buchneri CNCM I‐4323/NCIMB 40788 as a silage additive for all animal species

Safety and efficacy of Lactobacillus hilgardii CNCM I‐4785 and Lactobacillus buchneri CNCM I‐4323/NCIMB 40788 as a silage additive for all animal species

Published on: Tue, 30 Oct 2018 00:00:00 +0100 Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed was asked to deliver a scientific opinion on the safety and efficacy of a strain of Lactobacillus hilgardii and of Lactobacillus buchneri when used as a technological additive intended to improve ensiling at a proposed application rate of 3.0 x 108 colony forming units (CFU)/kg fresh material. The two bacterial species are considered by EFS...

Europe - EFSA - European Food Safety Authority Publications

24-10-2018

Safety and efficacy of Hostazym® X (endo‐1,4‐beta‐xylanase) as a feed additive for sows in order to have benefit in piglets

Safety and efficacy of Hostazym® X (endo‐1,4‐beta‐xylanase) as a feed additive for sows in order to have benefit in piglets

Published on: Tue, 23 Oct 2018 00:00:00 +0200 Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the safety and efficacy of HOSTAZYM® X as a feed additive for sows in order to have benefit in piglets. The additive HOSTAZYM® X contains endo‐1,4‐beta‐xylanase and is available in liquid and solid formulations. This product is authorised as a feed additive for chickens for fattening, tu...

Europe - EFSA - European Food Safety Authority Publications

20-10-2018

Scientific Opinion of Flavouring Group Evaluation 411 (FGE.411): 2‐(4‐methylphenoxy)‐N‐(1H‐pyrazol‐3‐yl)‐N‐(thiophen‐2‐ylmethyl)acetamide from chemical group 30 (miscellaneous substances)

Scientific Opinion of Flavouring Group Evaluation 411 (FGE.411): 2‐(4‐methylphenoxy)‐N‐(1H‐pyrazol‐3‐yl)‐N‐(thiophen‐2‐ylmethyl)acetamide from chemical group 30 (miscellaneous substances)

Published on: Fri, 19 Oct 2018 00:00:00 +0200 EFSA was requested to deliver a scientific opinion on the implications for human health of the flavouring substance 2‐(4‐methylphenoxy)‐N‐(1H‐pyrazol‐3‐yl)‐N‐(thiophen‐2‐ylmethyl)acetamide [FL‐no: 16.133], in the Flavouring Group Evaluation 411 (FGE.411), according to Regulation (EC) No 1331/2008 of the European Parliament and of the Council. The substance has not been reported to occur in natural source materials of botanical or animal origin. It is intende...

Europe - EFSA - European Food Safety Authority Publications

16-10-2018

Modification of the existing maximum residue levels for mepiquat in cotton seeds and animal commodities

Modification of the existing maximum residue levels for mepiquat in cotton seeds and animal commodities

Published on: Mon, 15 Oct 2018 00:00:00 +0200 In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant, BASF SE, submitted an application to the competent national authority in Greece to modify the existing maximum residue level (MRL) for the active substance mepiquat in cotton seeds. The data submitted in support of the application were found to be sufficient to derive a MRL proposal for cotton seeds and the previously derived MRL proposals for animal commodities were found to be stil...

Europe - EFSA - European Food Safety Authority Publications

11-10-2018

Re‐evaluation of oxidised soya bean oil interacted with mono‐ and diglycerides of fatty acids (E 479b) as a food additive

Re‐evaluation of oxidised soya bean oil interacted with mono‐ and diglycerides of fatty acids (E 479b) as a food additive

Published on: Wed, 10 Oct 2018 00:00:00 +0200 The EFSA Panel on Food Additives and Flavourings (FAF) provides a scientific opinion re‐evaluating the safety of thermally oxidised soya bean oil interacted with mono‐ and diglycerides of fatty acids (TOSOM) (E 479b) when used as a food additive. The Scientific Committee on Food (SCF) and the Joint FAO/WHO Expert Committee on Food Additives (JECFA) derived an acceptable daily intake (ADI) of 25 and 30 mg/kg body weight (bw) per day, respectively. There was n...

Europe - EFSA - European Food Safety Authority Publications

6-10-2018

Modification of the existing maximum residue level for epoxiconazole in beetroots

Modification of the existing maximum residue level for epoxiconazole in beetroots

Published on: Fri, 05 Oct 2018 00:00:00 +0200 In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Agriculture & Horticulture Development Board submitted a request to the competent national authority in the United Kingdom to modify the existing maximum residue level (MRL) for the active substance epoxiconazole in beetroots. The data submitted in support of the request were found to be sufficient to derive a MRL proposal for beetroots. Adequate analytical methods for enforcement are...

Europe - EFSA - European Food Safety Authority Publications

1-10-2018

Public Notification: FX75000 contains hidden drug ingredient

Public Notification: FX75000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use FX75000, a product promoted for sexual enhancement. This product was identified during an examination of international mail shipments.

FDA - U.S. Food and Drug Administration

27-9-2018

Outcome of the consultation on confirmatory data used in risk assessment for the active substance  copper (I), copper (II) variants

Outcome of the consultation on confirmatory data used in risk assessment for the active substance copper (I), copper (II) variants

Published on: Wed, 26 Sep 2018 00:00:00 +0200 The European Food Safety Authority (EFSA) was asked by the European Commission to provide scientific assistance with respect to the risk assessment for an active substance in light of confirmatory data requested following the first approval in accordance with Article 6(1) of Directive 91/414/EEC and Article 6(f) of Regulation (EC) No 1107/2009. In this context EFSA's scientific views on the specific points raised during the commenting phase conducted with Me...

Europe - EFSA - European Food Safety Authority Publications

19-9-2018

Modification of the existing maximum residue levels for flonicamid in various root crops

Modification of the existing maximum residue levels for flonicamid in various root crops

Published on: Tue, 18 Sep 2018 00:00:00 +0200 In accordance with Article 6 of Regulation (EC) No 396/2005, the Agriculture and Horticulture Development Council submitted a request to the competent national authority in the United Kingdom to modify the existing maximum residue levels (MRL) for the active substance flonicamid in beetroots, carrots, celeriacs/turnip rooted celeries, horseradishes, Jerusalem artichokes, parsnips, parsley roots/Hamburg roots parsley, radishes, salsifies, swedes/rutabagas, tu...

Europe - EFSA - European Food Safety Authority Publications

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

29-8-2018

Risk to human and animal health related to the presence of 4,15‐diacetoxyscirpenol in food and feed

Risk to human and animal health related to the presence of 4,15‐diacetoxyscirpenol in food and feed

Published on: Thu, 16 Aug 2018 00:00:00 +0200 4,15‐Diacetoxyscirpenol (DAS) is a mycotoxin primarily produced by Fusarium fungi and occurring predominantly in cereal grains. As requested by the European Commission, the EFSA Panel on Contaminants in the Food Chain (CONTAM) assessed the risk of DAS to human and animal health related to its presence in food and feed. Very limited information was available on toxicity and on toxicokinetics in experimental and farm animals. Due to the limitations in the avai...

Europe - EFSA - European Food Safety Authority Publications

29-8-2018

Setting of import tolerances for mandestrobin in strawberries and table and wine grapes

Setting of import tolerances for mandestrobin in strawberries and table and wine grapes

Published on: Thu, 16 Aug 2018 00:00:00 +0200 In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Sumitomo Chemical Agro Europe SAS submitted a request to the competent national authority in Austria to set an import tolerance for the active substance mandestrobin in strawberries, table grapes and wine grapes. The data submitted in support of the request were found to be sufficient to derive maximum residue level (MRL) proposals for the crops under consideration. Adequate analytica...

Europe - EFSA - European Food Safety Authority Publications

29-8-2018

Modification of the existing maximum residue levels for fluoxastrobin in oilseeds

Modification of the existing maximum residue levels for fluoxastrobin in oilseeds

Published on: Mon, 13 Aug 2018 00:00:00 +0200 In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Arysta LifeSciences SAS submitted a request to the competent national authority in the United Kingdom to modify the existing maximum residue levels (MRL) for the active substance fluoxastrobin in certain oilseeds. The data submitted in support of the request were found to be sufficient to derive MRL proposals for the oilseeds for which a modification was requested. Adequate analytical...

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

31-7-2018

Public Notification: Black Rhino 25000 contains hidden drug ingredient

Public Notification: Black Rhino 25000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Black 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

31-7-2018

Public Notification: Krazzy Rhino 25000 contains hidden drug ingredient

Public Notification: Krazzy Rhino 25000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Krazzy 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

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

31-7-2018

Public Notification: Platinum Rhino 25000 contains hidden drug ingredient

Public Notification: Platinum Rhino 25000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Platinum 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

25-7-2018

AMPI Recalls Limited Amount of Dry Whey Powder Because of Possible Health Risk

AMPI Recalls Limited Amount of Dry Whey Powder Because of Possible Health Risk

Associated Milk Producers Inc. (AMPI) of New Ulm, Minn., is recalling dry whey powder packaged in 50-pound and 25-kg bags that were produced at the cooperative’s Blair, Wis., dry whey plant from May 1-5, 2018; May 24-29, 2018; June 2-5, 2018; and June 7-14, 2018 due to the potential to be contaminated with Salmonella. This is a precautionary recall. All products shipped to the marketplace tested negative for Salmonella.

FDA - U.S. Food and Drug Administration

13-7-2018

Hospira Issues Voluntary Nationwide Recall of Daptomycin for Injection Lyophilized Powder for Solution, Due to Infusion Reactions

Hospira Issues Voluntary Nationwide Recall of Daptomycin for Injection Lyophilized Powder for Solution, Due to Infusion Reactions

Hospira, Inc., a Pfizer company, is voluntarily recalling 8 lots of Hospira’s Daptomycin for Injection 500 mg, Lyophilized Powder For Solution, Single Dose Vial (NDC 0409-0106-01) to the Hospital/Retail level. The product is being recalled due to adverse event reports indicative of infusion reactions.

FDA - U.S. Food and Drug Administration

10-7-2018

Preventieve HIV-remmers (PrEP) worden verstrekt voor een periode van vijf jaar

Preventieve HIV-remmers (PrEP) worden verstrekt voor een periode van vijf jaar

PrEP wordt binnen een onderzoekssetting voor een periode van vijf jaar verstrekt aan de hoogrisicogroep van mannen die seks hebben met mannen (MSM). Dat heeft minister Bruno Bruins (Medische Zorg) vandaag bekend gemaakt. Op basis van schattingen van het RIVM zullen ongeveer 6500 mannen hiervan gebruik gaan maken en kunnen hiermee  250 hiv-infecties per jaar worden voorkomen. Voor gebruikers gaat een eigen bijdrage gelden van maximaal 25%, dat komt overeen met ongeveer 12 euro per maand. Ook wordt hen gev...

Netherlands - Ministerie van Volksgezondheid, Welzijn en Sport

26-6-2018

Huish Outdoors recalls Oceanic and Hollis Scuba Diving Regulators

Huish Outdoors recalls Oceanic and Hollis Scuba Diving Regulators

The scuba diving regulators can restrict airflow at low tank pressures (below 500 psi), posing a drowning hazard to divers.

Health Canada

22-6-2018

Metronidazole intravenous infusion 500 mg/100 mL bag

Metronidazole intravenous infusion 500 mg/100 mL bag

Shortage and althernative supply of Metronidazole intravenous infusion 500 mg/100 mL bag

Therapeutic Goods Administration - Australia

20-6-2018

Public Notification: Black Stallion 35000 contains hidden drug ingredient

Public Notification: Black Stallion 35000 contains hidden drug ingredient

The Food and Drug Administration is advising consumers not to purchase or use Black Stallion 35000, 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

28-11-2018

PHEBURANE (Eurocept International BV)

PHEBURANE (Eurocept International BV)

PHEBURANE (Active substance: Sodium Phenylbutyrate) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8043 of Wed, 28 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2500/T/20

Europe -DG Health and Food Safety

20-11-2018

.@US_FDA issues Class I Medical Device Recall, the most serious type of recall: Beckman Coulter Life Sciences Beckman Coulter Life Sciences recalls the FC500 Series Flow Cytometers and EPICS XL Series Flow Cytometers. Find out more:  https://go.usa.gov/xP

.@US_FDA issues Class I Medical Device Recall, the most serious type of recall: Beckman Coulter Life Sciences Beckman Coulter Life Sciences recalls the FC500 Series Flow Cytometers and EPICS XL Series Flow Cytometers. Find out more: https://go.usa.gov/xP

. @US_FDA issues Class I Medical Device Recall, the most serious type of recall: Beckman Coulter Life Sciences Beckman Coulter Life Sciences recalls the FC500 Series Flow Cytometers and EPICS XL Series Flow Cytometers. Find out more: https://go.usa.gov/xPAtn  #MedicalDevice #FDA pic.twitter.com/6e064UQ2wg

FDA - U.S. Food and Drug Administration

4-9-2018

Abseamed (Medice Arzneimittel PUtter GmbH and Co KG)

Abseamed (Medice Arzneimittel PUtter GmbH and Co KG)

Abseamed (Active substance: epoetin alfa) - Centralised - 2-Monthly update - Commission Decision (2018)5860 of Tue, 04 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/727/WS/1406

Europe -DG Health and Food Safety

19-6-2018

Maviret (AbbVie Deutschland GmbH and Co. KG)

Maviret (AbbVie Deutschland GmbH and Co. KG)

Maviret (Active substance: glecaprevir / pibrentasvir) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3916 of Tue, 19 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4430/T/11

Europe -DG Health and Food Safety

11-6-2018

Viekirax (AbbVie Deutschland GmbH and Co. KG)

Viekirax (AbbVie Deutschland GmbH and Co. KG)

Viekirax (Active substance: ombitasvir / paritaprevir / ritonavir) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3766 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3839/T/45

Europe -DG Health and Food Safety

4-6-2018

Venclyxto (AbbVie Deutschland GmbH and Co. KG)

Venclyxto (AbbVie Deutschland GmbH and Co. KG)

Venclyxto (Active substance: venetoclax) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3633 of Mon, 04 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4106/T/12

Europe -DG Health and Food Safety

4-6-2018

Exviera (AbbVie Deutschland GmbH and Co. KG)

Exviera (AbbVie Deutschland GmbH and Co. KG)

Exviera (Active substance: dasabuvir) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3628 of Mon, 04 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3837/T/38

Europe -DG Health and Food Safety

29-5-2018

Norvir (AbbVie Deutschland GmbH and Co. KG)

Norvir (AbbVie Deutschland GmbH and Co. KG)

Norvir (Active substance: Ritonavir) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3340 of Tue, 29 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/127/T/149

Europe -DG Health and Food Safety

25-5-2018

Kaletra (AbbVie Deutschland GmbH and Co. KG)

Kaletra (AbbVie Deutschland GmbH and Co. KG)

Kaletra (Active substance: lopinavir / Ritonavir) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3282 of Fri, 25 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/368/T/169

Europe -DG Health and Food Safety