TRI-KOMBI LAWN WEEDER

Main information

  • Trade name:
  • CAMPBELL TRI-KOMBI LAWN WEEDER
  • Pharmaceutical form:
  • Aqueous
  • Units in package:
  • 250mL,500mL
  • Class:
  • AgChem
  • Medicine domain:
  • Equipment
  • Medicine type:
  • Agrochemical
  • Manufactured by:
  • COLIN CAMPBELL

Documents

Localization

  • Available in:
  • CAMPBELL TRI-KOMBI LAWN WEEDER
    Australia
  • Language:
  • English

Therapeutic information

  • Therapeutic group:
  • HOME GARDEN LAWN | LAWN - NEWLY SOWN
  • Therapeutic area:
  • Group I Herbicide
  • Therapeutic indications:
  • BINDY-EYE | CAT'S EAR OR FLATWEED | CHICKWEED | CLOVER | CREEPING OXALIS | DANDELION - TARAXACUM OFFICINALE | FAT HEN | FUMITORY | MALLOW | MOUSE-EAR CHICKWEED | PEARLWORT | RIBWORT, RIBGRASS OR LAMB'S TONGUE | STAGGER WEED | BINDII | BOGAN FLEA | CALOTIS HISPIDULA | CLOVER SORREL | COMMON CHICKWEED | COMMON DANDELION | COMMON PLANTAIN | ENGLISH DANDELION | EUROPEAN DANDELION | FIELD STACHYS | HEDGE-NETTLE | JO-JO | MINT WEED | MOUSE-EARED CHICKWEED | NARROW LEAF PLANTAIN | ONEHUNGA WEED | PINK WEED | PROCUMBENT PEARLWORT | SAGINA APETALA | SAGINA PROCUMBENS | SMALL-LEAVED OXALIS | SPREADING PEARLWORT | STACHYS ORIENTALIS | STAR BURR | TARAXACUM SPP. | TRUE DANDELION | WHITE GOOSEFOOT | WOOD SORREL (YELLOW) | YELLOW WOOD SORREL
  • Product summary:
  • For the control of broadleaved weeds such as clovers and creeping oxalis, pearlwort, chickweed, mouse eared chickweed, lambs tongue, dandelions, catsear, fat hen, mallow, stagger weeds, fumitory and bindii in the home lawn.DO NOT mow turf for two days before or after treatment. DO NOT use on Buffalo lawns. DO NOT use in high winds

Other information

Status

  • Source:
  • Australian Pesticides and Veterinary Medicines Authority (APVMA)
  • Authorization status:
  • Registered and available
  • Authorization number:
  • 31537/0507
  • Authorization date:
  • 26-03-2008
  • Last update:
  • 15-06-2017

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

108mm

115mm

70mm

75mm

Scale 1:100

pms colours 2

black

red **please specify

Print size:

Front:108mm x 70mm

back: 115mm x 75mm

centered justified

white 250ml bottle

31537_42000_250mL_LABEL_V.02

Prints 100% on A4

APPROVED

LABEL

Info

pest

Verified

HOW TO PREPARE: Best results are obtained when the spray is applied

to actively growing weeds and the soil is moist. Application may be made

using a watering can with a fine rose.

STORAGE AND 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.

CAUTION: Do not feed grass clippings from treated areas to poultry or

other animals. DO NOT allow spray to contact or drift onto plants you do

not want killed.

DO NOT allow chemical containers or spray to get into

drains, sewers, streams or ponds.

SAFETY DIRECTIONS : Poisonous if swallowed. Avoid contact with eyes

and skin. May irritate the eyes, nose and throat and skin. Do not inhale

spray mist. If product on skin, immediately wash area with soap and water.

If product in eyes, wash it out immediately with water. After use and before

eating, drinking or smoking, wash hands, arms and face thoroughly with

soap and water.

FIRST AID : If poisoning occurs, contact a doctor or Poisons Information

Centre.

Phone 131126.

If skin contact

occurs, remove contaminated clothing

and wash skin thoroughly.

If in eyes,

hold eyes open, flood with water for at

least 15 minutes and see a doctor.

CONDITIONS

OF

SALE:

buyer

relies

entirely

skill

judgement in purchasing this product

and in deciding that it may be suitable

for the abovementioned purpose.

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

CONTRARY TO THIS LABEL UNLESS AUTHORISED

POISON

KEEP OUT OF REACH OF CHILDREN

READ SAFETY DIRECTIONS BEFORE OPENING OR USING

ACTIVE CONSTITUENTS:

336 g/L MECOPROP PRESENT AS THE DIMETHYLAMINE SALT

80 g/L 2,4-D PRESENT AS THE DIMETHYLAMINE

AND DIETHANOLAMINE SALTS

40g/L DICAMBA PRESENT AS THE DIMETHYLAMINE SALT

Claims for use

For control of broad-leaved weeds such as clovers and creeping oxalis

pearlwort, chickweed, mouse-eared chickweed, Iambs tongue, dandelion,

catsear, fat-hen, mallow, stagger weeds, fumitory and bindi-i in the

home lawn.

Distributed by

COLIN CAMPBELL (CHEMICALS) PTY LTD.

5 Blackfriar Place, Wetherill Park, NSW 2164

Telephone (02) 9725 2544

CONTENTS : 500mL

APVMA Approval No.: 31537/500mL/0507

Batch No.:

Date of Manufacture

TRI-KOMBI

LAWN WEEDER

Contents

Cover

1100m

2

HOW TO USE:

DO NOT mow turf for two days before or after treatment.

DO NOT use on Buffalo lawns.

DO NOT use in high winds.

Areas

Weeds Controlled

Broadleaved weeds

such as clovers,

creeping oxalis,

pearlwort, chickweed,

mouse-eared

chickweed, lambs

tongue, dandelion,

catsear, fat-hen,

mallow, stagger

weeds, fumitory and

bindi-i

Home lawns

Newly sown

turf

22 mL

(4 capfuls) in

10 litres of

water to

50 square

metres.

15 mL

(3 capfuls) in

10 litres of

water to

50 square

metres.

Do not apply

until 4 weeks

after first

mowing.

Repeat

application

7-14 days if

necessary.

Rate

How to apply

Kills

Bindi-i

Lawn Weeder_050707

31537_42000_500mL_LABEL_V.02

Prints 100% on A4

APPROVED

LABEL

4-12-2018

Mylan Expands Its Voluntary Nationwide Recall of Valsartan Tablets, USP, Amlodipine and Valsartan Tablets, USP, and Valsartan and Hydrochlorothiazide Tablets, USP, to all Lots Within Expiry Due to The Detection of Trace Amounts of NDEA (N-Nitrosodiethylam

Mylan Expands Its Voluntary Nationwide Recall of Valsartan Tablets, USP, Amlodipine and Valsartan Tablets, USP, and Valsartan and Hydrochlorothiazide Tablets, USP, to all Lots Within Expiry Due to The Detection of Trace Amounts of NDEA (N-Nitrosodiethylam

– Mylan N.V. (NASDAQ: MYL) today announced that its U.S. based Mylan Pharmaceuticals business is expanding its consumer-level voluntary nationwide recall to include all lots of Valsartan-containing products within expiry. The 104 additional lots include 26 lots of Amlodipine and Valsartan Tablets, USP (including the 5mg/160mg, 10mg/160mg, 5mg/320mg and 10mg/320mg strengths), 51 lots of Valsartan Tablets, USP (including 40 mg, 80 mg, 160 mg and 320 mg strengths), and 27 lots of Valsartan and Hydrochloroth...

FDA - U.S. Food and Drug Administration

28-11-2018

Information Update - Mylan-Valsartan medications voluntarily recalled as a precaution due to an impurity

Information Update - Mylan-Valsartan medications voluntarily recalled as a precaution due to an impurity

Mylan Pharmaceuticals ULC is voluntarily recalling four lots of Mylan-Valsartan tablets (40 mg, 80 mg, 160 mg and 320 mg strength) after testing found low levels of an impurity, N-nitrosodiethylamine (NDEA).

Health Canada

21-11-2018

Mylan Initiates Voluntary Nationwide Recall of 15 Lots of Valsartan Tablets, USP, Amlodipine and Valsartan Tablets, USP, and Valsartan and Hydrochlorothiazide Tablets, USP, Due to the Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Fou

Mylan Initiates Voluntary Nationwide Recall of 15 Lots of Valsartan Tablets, USP, Amlodipine and Valsartan Tablets, USP, and Valsartan and Hydrochlorothiazide Tablets, USP, Due to the Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Fou

Mylan N.V. (NASDAQ: MYL) today announced that its U.S. based Mylan Pharmaceuticals business is conducting a voluntary nationwide recall to the consumer level of select lots of Valsartan-containing products, including six lots of Amlodipine and Valsartan Tablets, USP (including the 5mg/160mg, 10mg/160mg, and 10mg/320mg strengths), seven lots of Valsartan Tablets, USP (including 40 mg, 80 mg, 160 mg, and 320 mg strengths), and two lots of Valsartan and Hydrochlorothiazide Tablets, USP 320mg/25mg strength. ...

FDA - U.S. Food and Drug Administration

9-8-2018

Camber Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Valsartan Tablets, USP, 40mg, 80mg, 160mg and 320mg Due to The Detection of Trace Amounts of N-Nitrosodimethylamine (NDMA) Impurity, Found in an Active Pharmaceutical Ingredient (API)

Camber Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Valsartan Tablets, USP, 40mg, 80mg, 160mg and 320mg Due to The Detection of Trace Amounts of N-Nitrosodimethylamine (NDMA) Impurity, Found in an Active Pharmaceutical Ingredient (API)

As a precautionary measure, Camber Pharmaceuticals, Inc. is voluntarily recalling all unexpired lots of Valsartan Tablets, USP, 40mg, 80mg, 160mg and 320mg to the hospital, retail and consumer level. This recall of multiple batches of Valsartan Tablets was prompted due to the detection of trace amounts of N-Nitrosodimethylamine (NDMA), a possible process impurity or contaminant in an active pharmaceutical ingredient, manufactured by Hetero Labs Limited, Unit – I (API manufacturer).

FDA - U.S. Food and Drug Administration

13-7-2018

Prinston Pharmaceutical Inc Issues Voluntary Nationwide Recall of Valsartan and Valsartan HCTZ Tablets Due to Detection of a Trace Amount of Unexpected Impurity, N-Nitrosodimethylamine (NDMA) in The Products

Prinston Pharmaceutical Inc Issues Voluntary Nationwide Recall of Valsartan and Valsartan HCTZ Tablets Due to Detection of a Trace Amount of Unexpected Impurity, N-Nitrosodimethylamine (NDMA) in The Products

Prinston Pharmaceutical Inc. dba Solco Healthcare LLC. is recalling all lots of Valsartan Tablets, 40 mg, 80mg, 160mg, and 320mg; and Valsartan-Hydrochlorothiazide Tablets, 80mg/12.5mg, 160mg/12.5mg, 160mg/25mg, 320mg/12.5mg, and 320mg/25mg to the retail level. This product recall is due to the detection of a trace amount of an unexpected impurity, N-nitrosodimethylamine (NDMA), made by the manufacturer – Zhejiang Huahai Pharmaceutical Co. Ltd. -- that is used in the manufacture of the subject product ...

FDA - U.S. Food and Drug Administration

29-6-2018

High doses of MDMA can lead to a spike in body temperature that can result in heart failure or even death.  https://www.drugabuse.gov/publications/drugfacts/mdma-ecstasymolly …
#DrugFacts #FridayFactspic.twitter.com/tPDHYkvW43

High doses of MDMA can lead to a spike in body temperature that can result in heart failure or even death. https://www.drugabuse.gov/publications/drugfacts/mdma-ecstasymolly … #DrugFacts #FridayFactspic.twitter.com/tPDHYkvW43

High doses of MDMA can lead to a spike in body temperature that can result in heart failure or even death. https://www.drugabuse.gov/publications/drugfacts/mdma-ecstasymolly … #DrugFacts #FridayFacts pic.twitter.com/tPDHYkvW43

FDA - U.S. Food and Drug Administration