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Betamox Amoxycillin Antibiotic

Betamox Amoxycillin Antibiotic
200mg Tablets » Priced per Tablet
Injection » 100ml Bottle
Palatable Drops » 15ml Bottle

  • 200mg Tablets » Priced per Tablet £0.79
  • Injection » 100ml Bottle £23.50
  • LA Injection » 100ml Bottle £23.99
  • Palatable Drops » 15ml Bottle £10.49

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£0.79 to £23.99

Description

Amoxycillin is used for the treatment of infections caused by a wide range of Gram-positive and Gram-negative pathogenic bacteria including:
Actinobacillus equuli, Actinomyces bovis, Actinobacillus lignieresi, Bacillus anthracis, rysipelothrix rhusiopathiae, Bordetella bronchiseptica, Escherichia coli, Clostridium species, Haemophilus species, Coryne bacterium species, Pasteurella species, Fusiformis species, Proteus mirabilis, Moraxella species, Salmonella species and Staphylococci Streptococci
It is not effective against beta-lactamase producing (penicillin resistant) organisms.
Only to be used when prescribed by your vet.

For the treatment of infections caused by the wide range of Gram-positive and Gram-negative pathogenic bacteria including:
Actinobacillus equuli, Actinomyces bovis, Actinobacillus lignieresi, Bacillus anthracis, rysipelothrix rhusiopathiae, Bordetella bronchiseptica, Escherichia coli, Clostridium species, Haemophilus species, Coryne bacterium species, Pasteurella species, Fusiformis species, Proteus mirabilis, Moraxella species, Salmonella species and Staphylococci Streptococci

Not effective against beta-lactamase producing organisms.

Only to be used when prescribed by your vet.

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All prices include VAT where applicable.

Medication Datasheets

Injection » 100ml Bottle

SUMMARY OF PRODUCT CHARACTERISTICS

  1. Name of the veterinary medicinal product

    Betamox 150 mg/ml Suspension for Injection

  2. Qualitative and quantitative composition

Each ml contains

Active Substance: Amoxicillin 150 mg (as Amoxicillin Trihydrate 172.1 mg)

Excipients: Butylated Hydroxyanisole 0.08 mg Butylated Hydroxytoluene 0.08 mg

For a full list of excipients, see section 6.1

  1. Pharmaceutical form

Suspension for injection.
An off-white oily suspension.

  1. Clinical Particulars

4.1 Target species

Cattle
Sheep
Pigs
Dogs
Cats

4.2 Indications for use, specifying the target species

For the treatment of infections caused by a wide range of Gram-positive and Gram-negative pathogenic bacteria including:

Actinobacillus equuli    Actinomyces bovis
Actinobacillus lignieresi    Bacillus anthracis
Erysipelothrix rhusiopathiae    Bordetella bronchiseptica
Escherichia coli    Clostridium species
Haemophilus species    Corynebacterium species
Pasteurella species    Fusiformis species
Proteus mirabilis    Moraxella species
Salmonella species
Staphylococci

Streptococci Not effective against beta-lactamase producing organisms. 4.3 Contraindications

Intravenous or intrathecal use.
Use in rabbits, hamsters, gerbils and guinea pigs.
Use in known cases of hypersensitivity to amoxycillin.

4.4 Special Warnings for each target species

None

4.5 Special precautions for use

Special precautions for use in animals

None

Special precautions to be taken by the person administering the veterinary medicinal product to animals

Care should be taken to avoid accidental self-injection. In the case of accidental self-injection, seek medical advice immediately. Penicillins and cephalosporins may cause hypersensitivity (allergy) following injection, inhalation, ingestion or skin contact. Hypersensitivity to penicillins may lead to cross reactions to cephalosporins and vice versa. Allergic reactions to these substances may occasionally be serious.

Do not handle this product if you know you are sensitised, or if you have been advised not to work with such preparations

Handle this product with great care to avoid exposure taking all recommended precautions.

If you develop symptoms following exposure, such as a skin rash, you should seek medical advice and show the doctor this warning. Swelling of the face, lips or eyes or difficulty breathing are more serious symptoms and require urgent medical attention.

Wash hands after use.

4.6 Adverse reactions (frequency and seriousness)

Occasional local tissue reactions may result from use of this product.

4.7 Use during pregnancy, lactation or lay

Betamox Injection can be safely administered during pregnancy and lactation.

4.8 Interaction with other medicinal products and other forms of interaction

None known.

4.9 Amounts to be administered and administration route

Cattle, sheep and pigs    :    By intramuscular injection only.
Dogs and cats    :    By subcutaneous or intramuscular injection.

The recommended dosage rate is 7 mg/kg bodyweight once a day for up to five days.  Massage the injection site.

A separate injection site should be used for each administration.

Animal Weight (kg) Dose volume (ml) Cattle 450 20.0 Sheep 65 3.0 Pigs 150 7.0 Dogs 20 1.0 Cats 5 0.25 (Guide-dose volume is equivalent to about 0.25 ml per 5 kg daily).

Normal aseptic precautions should be observed.  Shake vial before use. This product does not contain an antimicrobial preservative. Swab the septum before removing each dose. Use a dry, sterile needle and syringe.

If dose volume exceeds 20 ml in cattle or 10 ml in pigs, it should be divided and injected into two sites.  

Overdose (symptoms, emergency procedures, antidotes), if necessary

Penicillin’s have a wide safety margin

Withdrawal period

Milk for human consumption must not be taken from a cow during treatment.  Milk for human consumption may only be taken after 24 hours from the last treatment.

Not for use in sheep producing milk for human consumption.

Animals must not be slaughtered for human consumption during treatment.  Cattle may be slaughtered for human consumption only after 18 days from the last treatment.  Sheep may be slaughtered for human consumption only after 10 days from the last treatment.  Pigs may be slaughtered for human consumption only after 16 days from the last treatment.
  1. pharmacological properties

Pharmacotherapeutic group: Antibiotic

ATC Vet Code: QJ 01 CA 04

5.1 Pharmacodynamic properties

Amoxycillin predominately inhibits cell wall synthesis in susceptible bacteria.  Amoxycillin has a unique mode of action which directly and irreversibly disrupts existing cell wall peptidoglycan rather than newly forming peptidoglycan of the divisory septal wall as with other members of the penicillin family.    
  1. Pharmaceutical particulars

6.1 List of excipients

Butylated Hydroxyanisole
Butylated Hydroxytoluene
Aluminium Stearate

Propylene Glycol Dicaprylocaprate

6.2 Incompatibilities

None known

Shelf-life

Shelf life of the veterinary medicinal product as packaged for sale: 2 years Shelf life after first opening the immediate packaging: 28 days

6.4 Special precautions for storage

Following withdrawal of the first dose, use the product within 28 days. Discard unused material.

Do not store above 25ºC.

6.5 Nature and composition of immediate packaging

Betamox Injection is supplied in 50 ml and 100 ml clear, colourless Type III or Type II glass vials, closed with nitrile rubber bungs and aluminium overseals, and 50 ml and 100 ml clear plastic vials closed with nitrile rubber bungs and aluminium overseals.
Not all pack sizes may be marketed.

6.6 Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products

Any unused veterianry medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with the local requirements.  
  1. MARKETING AUTHORISATION HOLDER

    Norbrook Laboratories Limited Station Works Camlough Road Newry Co. Down BT35 6JP Northern Ireland

  2. MARKETING AUTHORISATION NUMBER

    Vm 02000/4071

  3. DATE OF FIRST AUTHORISATION

    Date: 30 June 1986

  4. DATE OF REVISION OF THE TEXT

    Date: October 2014

APPROVED 23/10/14

LA Injection » 100ml Bottle

SUMMARY OF PRODUCT CHARACTERISTICS

  1. Name of the veterinary medicinal product

    Betamox LA 150 mg/ml Suspension for Injection

  2. Qualitative and quantitative composition

Active Substance: Each ml contains: 150 mg (15% w/v) Amoxicillin (as Amoxicillin Trihydrate 17.21 %w/v),

Excipients: 0.08 mg (0.008% w/v) butylated hydroxytoluene 0.08 mg (0.008% w/v) butylated hydroxyanisole as antioxidants.

For a full list of excipients, see section 6.1

  1. Pharmaceutical form

    Suspension for injection. An off-white oily non-aqueous suspension.

  2. Clinical Particulars

4.1 Target species

Cattle, Sheep, Pigs, Dogs, Cats

4.2 Indications for use, specifying the target species

In vitro Amoxicillin is effective against a wide range of Gram-positive and Gram-negative bacteria which include:

Escherichia coli
Klebsiella pneumoniae
Proteus species
Salmonella species
Staphylococci and
Streptococci

Not effective against beta-lactamase producing organisms.

Suitable for the control of infections due to susceptible microorganisms in cattle, sheep, pigs, dogs and cats where a single injection giving prolonged activity is required.  It may also protect from secondary bacterial invasion due to sensitive organisms in cases where bacteria are not the initial cause of the disease.
Indications include infections of:

(a)    Alimentary tract
(b)    Respiratory tract
(c)    Skin and soft tissue
(d)    Urogenital tract and,
(e)    In prevention of post-operative infection (treat before surgery).

4.3 Contraindications

This product is not suitable for intravenous or intrathecal use

This product should not be administered to rabbits, hamsters, gerbils or guinea pigs.

Not for use in known cases of hypersensitivity to penicillins or cephalosporins.

4.4 Special Warnings for each target species

No special warnings.

4.5 Special precautions for use

Special precautions for use in animals

Use of the product should be based on susceptability testing of the bacteria isolated from the animal. If this is not posible, therapy should be based on local epidemiological information.

Special precautions to be taken by the person administering the veterinary medicinal product to animals

Care should be taken to avoid accidental self-injection. In the case of accidental self-injection, seek medical advice immediately.

Penicillins and cephalosporins may cause hypersensitivity (allergy) following injection, inhalation, ingestion or skin contact. Hypersensitivity to penicillins may lead to cross-reactions to cephalosporins and vice versa. Allergic reactions to these substances may occasionally be serious.

  1. Do not handle this product if you know you are sensitised, or if you have been advised not to work with such preparations.

  2. Handle this product with great care to avoid exposure, taking all recommended precautions.

  3. If you develop symptoms following exposure such as skin rash, you should seek medical advice and show the doctor this warning. Swelling of the face, lips or eyes or difficulty with breathing, are more serious symptoms and require urgent medical attention. Wash hands after use.

4.6 Adverse reactions (frequency and seriousness)

Occasional local tissue reaction may result from injection.

4.7 Use during pregnancy, lactation or lay

Can be safely administered during pregnancy and lactation.

4.8 Interaction with other medicinal products and other forms of interaction

It is not generally recommended to use bactericidal and bacteriostatic antibiotics at the same time.

4.9 Amounts to be administered and administration route

To ensure the correct dosage, bodyweight should be determined as accurately as possible to avoid underdosing.

Cattle, sheep and pigs - By intramuscular injection only.

Dogs and cats - By subcutaneous or intramuscular injection.

The recommended dosage rate is 15 mg per kg bodyweight, repeatable if necessary after 48 hours. Massage the injection site. Shake the vial before use Swab the septum before removing each dose. Use a dry sterile needle and syringe. A separate injection site should be used for each administration.

Animal Weight (kg) Dosage volume (ml) Cattle 450 kg 45.0 ml Sheep 65 kg 6.5 ml Pigs 150 kg 15.0 ml Dogs 20 kg 2.0 ml Cats 5 kg 0.5 ml

Dose volume is equivalent to 1 ml per 10 kg bodyweight. If dose volume exceeds 20 ml, it should be divided and injected into two sites. As with other injectable preparations normal aseptic precautions should be observed. An appropriately graduated syringe must be used to allow accurate administration of the required dose volume. This is particularly important when injecting small volumes.

Overdose (symptoms, emergency procedures, antidotes), if necessary

Penicillins have a wide safety margin.

Withdrawal period

Milk for human consumption must not be taken from a cow during treatment. With cows milked twice daily, milk for human consumption may only be taken from 79 hours (i.e. at the 7th milking) after the last treatment. With other dosing routines, the basis of the veterinary surgeons advice should be that milk may be taken for human consumption only after the same period from the last treatment (i.e. with three times a day milking, milk for human consumption may only be taken at the 10th milking).

Cattle (meat): 23 days from the last treatment. Sheep and pigs (meat): 16 days from the last treatment.

Not for use in sheep producing milk for human consumption.

  1. pharmacological properties

Pharmacotherapeutic group: Antibacterial

ATC Vet Code: QJ01CA04

Pharmacodynamic properties

Amoxicillin predominately inhibits cell wall synthesis in susceptible bacteria. Amoxicillin has a unique mode of action which directly and irreversibly disrupts existing cell wall peptidoglycan rather than newly forming peptidoglycan of the divisory septal wall as with other members of the penicillin family.

  1. Pharmaceutical particulars

List of excipients

Butylated Hydroxyanisole Butylated Hydroxytoluene Aluminium Stearate Propylene Glycol Dicaprylocaprate

Incompatibilities

None known

Shelf life

Shelf life of the veterinary medicinal product as packaged for sale: 2 years.

Shelf life after first opening the immediate packaging: 28 days

Special precautions for storage

Do not store above 25ºC. 

Protect from light.
Following withdrawal of the first dose, use the product within 28 days. Discard unused material. This product does not contain an antimicrobial preservative.

Nature and composition of immediate packaging

100 ml and 50 ml clear, colourless Type II or III multidose glass vials, closed with nitrile rubber bungs and aluminium overseals. 50 ml, 100 ml, 250 ml and 500 ml clear polyethylene terephthalate vials sealed with nitryl bungs and aluminium overseals.

Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products

Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.

  1. MARKETING AUTHORISATION HOLDER

Norbrook Laboratories Limited Station Works Camlough Road Newry Co. Down BT35 6JP Northern Ireland

  1. MARKETING AUTHORISATION NUMBER

Vm 02000/4070

  1. DATE OF FIRST AUTHORISATION

    Date: 30 July 1986

  2. DATE OF REVISION OF THE TEXT

Date: October 2014

APPROVED 23/10/14

Palatable Drops » 15ml Bottle

  1. Name of the veterinary medicinal product

    Betamox Palatable Drops, Powder for Oral Suspension 50 mg/ml

Qualitative and quantitative composition

Each bottle contains:

Active Substance: mg Amoxicillin…………………………………………750 (as Amoxicillin Trihydrate)

When reconstituted with 12 ml water gives a 15 ml suspension containing amoxicillin at a concentration of 50 mg/ml.

Excipients:

Erythrosin E127 …………………………………..2.34 For a full list of excipients, see section 6.1

  1. Pharmaceutical form

    Powder for oral suspension A pale red powder

  2. Clinical Particulars

4.1 Target species

Dogs
    Cats

4.2 Indications for use, specifying the target species

For the control of infections in dogs and cats, including infections of the alimentary tract, respiratory tract and urogenital tract, eye and ear infections, and skin and wound infections.  In vitro, amoxycillin is effective against a wide range of Gram-positive and Gram-negative bacteria, including:

Bacillus cereus
Bordetella bronchiseptica
Corynebacterium spp
Citrobacter freundii
Chromobacter spp
Escherichia coli
Flavobacter spp
Pasteurella spp (including P. multocida)
Proteus mirabilis
Salmonella spp
Staphylococci (penicillin sensitive stains)
Streptococci

4.3 Contraindications

Not to be used in animals known to be hypersensitive to penicillin.

Not to be used orally or parenterally in rabbits, guinea pigs, hamsters or gerbils.

Caution is advised when used in any other small herbivores.

4.4 Special Warnings for each target species

No special warnings

4.5 Special precautions for use

Special precautions for use in animals

Use of the product should be based on susceptibility testing of the bacteria isolated from the animal. If this is not possible, therapy should be based on local epidemiological information.

Special precautions to be taken by the person administering the veterinary medicinal product to animals

Penicillins and cephalosporins may cause hypersensitivity (allergy) following injection, inhalation, ingestion or skin contact. Hypersensitivity to penicillins may lead to cross reactions to cephalosporins and vice versa. Allergic reactions to these substances may occasionally be serious.

  1. Do not handle this product if you know you are sensitised, or if you have been advised not to work with such preparations.
  2. Handle this product with great care to avoid exposure, taking all recommended precautions.
  3. If you develop symptoms following exposure such as a skin rash, you should seek medical advice and show the doctor this warning. Swelling of the face, lips or eyes or difficulty with breathing are more serious symptoms and require urgent medical attention.

    Wash hands after use. 4.6 Adverse reactions (frequency and seriousness) No known undesirable effects

4.7 Use during pregnancy, lactation or lay No known contraindication exists for the use of Betamox Palatable Drops during pregnancy.

4.8 Interaction with other medicinal products and other forms of interaction None known. 4.9 Amounts to be administered and administration route Reconstitution: Add 12 ml water to the powder and shake vigorously. This will make 15 ml of the suspension, containing amoxycillin at a concentration of 50 mg/ml. Administration and Dosage: Recommended dosage rate is 10 mg/kg bodyweight amoxycillin twice daily for up to 7 days. The drops are given orally using a graduated pipette provided. The dosage rate of 10 mg/kg is achieved by administering 1 ml of reconstituted product per 5 kg bodyweight.

Shake well before use

To ensure the correct dosage, bodyweight should be determined as accurately as possible to avoid under dosing.

Overdose (symptoms, emergency procedures, antidotes), if necessary Penicillins have a high margin of safety and clinical signs are unlikely even in accidental overdose.

No treatment specified.

Withdrawal period

Not applicable 5. pharmacological properties

Pharmacotherapeutic group: Antibacterial

ATC Vet Code: QJ01CA04

Pharmacodynamic properties

Amoxycillin is a broad-spectrum semi-synthetic penicillin. Amoxycillin predominately inhibits cell wall synthesis in susceptible bacteria. Amoxycillin has a mode of action which directly and irreversibly disrupts cell wall peptidoglycan. Amoxicillin is absorbed well after oral administration, giving high plasma and tissue levels. Excretion takes place in both bile and urine.

  1. Pharmaceutical particulars

List of excipients

Erythrosine (E127) Trusil Strawberry Select Flavour H9922 Lactose Monohydrate

Incompatibilities

None known

Shelf life

Shelf-life of the veterinary medicinal product as packaged for sale: 2 years.

Shelf life after dilution or reconstitution according to direction: 7 days

Special precautions for storage

Do not store above 25ºC. Do not store reconstituted product above 25ºC.
Any reconstituted product remaining 7 days after preparation should be discarded

Nature and composition of immediate packaging

White polyethylene / polypropylene bottle with white, wadded polypropylene cap (screw-fit), with a graduated natural polyethylene pipette with white polypropylene screw-on cap and natural rubber bulb as a dosing device. 

Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products

Any unused veterinary medicinal product or waste materials derived form such veterinary medicinal products should be disposed of in accordance with local requirements.

  1. MARKETING AUTHORISATION HOLDER

Norbrook Laboratories Limited Station Works Newry Co. Down, BT35 6JP Northern Ireland

  1. MARKETING AUTHORISATION NUMBER(S)

    Vm: 02000/4101

DATE OF FIRST AUTHORISATION

  25th February 1988
  1. DATE OF REVISION OF THE TEXT

    December 2008

200mg Tablets » Priced per Tablet

SUMMARY OF PRODUCT CHARACTERISTICS

  1. Name of the veterinary medicinal product

    Betamox 200mg Palatable Tablets

  2. Qualitative and quantitative composition

Each tablet contains:

Active Substance: Amoxicillin 200 mg (as Amoxicillin Trihydrate 229.7 mg)

Excipients: For a full list of excipients, see section 6.1

  1. Pharmaceutical form

    Tablet Off-white circular tablets scored on one face

  2. Clinical Particulars

4.1 Target species

Dogs
Cats

4.2 Indications for use, specifying the target species

For use in the treatment of bacterial infections of the alimentary, respiratory and urogenital tracts and in the eye, ear, skin and wound infections caused by susceptible organisms.  In vitro, amoxicillin is effective against a range of Gram-positive and Gram-negative bacteria, including:

Bacillus cereus
Bordetella bronchiseptica
Corynebacterium spp
Chromobacter spp
Citrobacter freundii
Escherichia coli
Flavobacter spp
Proteus mirabilis
Pasteurella spp including Pasteurella multocida
Salmonella spp
Staphylococci (penicillin sensitive strains)
Streptococci

4.3 Contraindications

Betamox 200mg Palatable Tablets should not be given to penicillin sensitive animals.  As with other penicillins, amoxicillin should not be used orally or parenterally in rabbits, guinea pigs, hamsters or gerbils.  Caution is advised when used in other very small herbivores.

4.4 Special Warnings for each target species

No special warnings.

4.5 Special precautions for use

Special precautions for use in animals

No special precautions for use

Special precautions to be taken by the person administering the veterinary medicinal product to animals

Penicillins and cephalosporins may cause hypersensitivity (allergy) following injection, inhalation, ingestion or skin contact. Hypersensitivity to penicillins may lead to cross-reactions to cephalosporins and vice versa. Allergic reactions to these substances may occasionally be serious.

  1. Do not handle this product if you know you are sensitised, or if you have been advised not to work with such preparations.
  2. Handle this product with great care to avoid exposure, taking all recommended precautions.
  3. If you develop symptoms following exposure such as a skin rash, you should seek medical advice and show the doctor this warning. Swelling of the face, lips or eyes or difficulty with breathing are more serious symptoms and require urgent medical attention.

Wash hands after use

4.6 Adverse reactions (frequency and seriousness)

No known undesirable effects.

4.7 Use during pregnancy, lactation or lay

No known contraindication exists for use of Betamox 200 mg Palatable Tablets during pregnancy.

4.8 Interaction with other medicinal products and other forms of interaction

None known

4.9 Amounts to be administered and administration route

The recommended dose rate is 10 mg amoxicillin per kg bodyweight (one tablet per 20 kg bodyweight) twice daily for 7 days.

Tablets are given orally by hand or crushed in food.

Any remaining medicated feed should be disposed of at the end of the day.

Overdose (symptoms, emergency procedures, antidotes), if necessary

No treatment specified

Withdrawal period

Not applicable.

  1. pharmacological properties

Pharmacotherapeutic group: Antibiotic

ATC Vet Code: QJ01CA04

5.1 Pharmacodynamic properties

Amoxicillin is a broad-spectrum semi-synthetic penicillin. Amoxicillin predominately inhibits cell wall synthesis in susceptible bacteria.  Amoxicillin has a mode of action which directly and irreversibly disrupts cell wall peptidoglycan.  
  1. Pharmaceutical particulars

6.1 List of excipients

Cellulose Microcrystalline
Lactose Monohydrate
Sodium Glycollate Type A
Povidone K17
Yeast Dried (Spray Dried)
Magnesium Stearate

6.2 Incompatibilities

None known

6.3 Shelf-life

Shelf life of the veterinary medicinal product as packaged for sale: 2 years

6.4 Special precautions for storage

Do not store above 25ºC.  

Store in a dry place

6.5 Nature and composition of immediate packaging

Betamox 200 mg Palatable Tablets are supplied in white opaque high density polypropylene tubs with white opaque push-fit low density polyethylene caps of the following sizes:

100 x Betamox 200 mg Tablets
250 x Betamox 200 mg Tablets

Not all pack sizes may be marketed

6.6 Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products

Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements.
  1. MARKETING AUTHORISATION HOLDER

    Norbrook Laboratories Limited Station Works Newry Co. Down, BT35 6JP Northern Ireland

  2. MARKETING AUTHORISATION NUMBER(S)

    Vm 02000/4103

  3. DATE OF FIRST AUTHORISATION

    17th November 1987

  4. DATE OF REVISION OF THE TEXT

July 2010

Delivery Information

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Under almost all products on our website is an Estimated dispatch time, check this for a delivery prediction specific to the item you are looking to purchase. These badges are updated live based on the stock levels we have and also those of our suppliers - so are usually very accurate, but cannot be guaranteed. In more general terms, we aim to dispatch all orders within 1 working day of receiving payment (and a prescription if required). If we cannot do so within 3 working days we will contact you by email.

What do you charge for delivery?

For UK delivery, we charge the following:

Order Total Weight Delivery
£0-£28.99 Under 2kg £2.99
2kg+ £4.99
£29-£38.99 Under 2kg Free
2kg+ £4.99
£39+ Under 2kg Free
2kg+ Free

Prices quoted are for delivery to all parts of mainland UK except certain Scottish postcodes (where the price is higher for items sent by courier. Delivery of food abroad (including Channel Islands, N. Ireland and other islands around the UK) is charged at a higher price and free delivery is not available. Temperature controlled products, such as Insulin, are also not always subject to the standard and/or free delivery options.

For full information on our delivery charges, including prices on heavy deliveries to Scotland and abroad, see our delivery information page.

We can deliver most items to all around the world, but prices do vary. The majority of light weight orders (less than 1.5kg) can be delivered for a flat rate of £10. For an accurate estimate of the delivery charge, please put the items you require in your basket and use the "Estimate Delivery" system on the shopping basket page (you only need to enter your country and postal/zip code) for a quick quote. For deliveries to the USA you may need to go to the checkout page and enter your full address to get a quote (as some services need your state in order to quote too). For more information on international deliveries, please see our delivery information page.

Delivery of aerosols

Due to restrictions aerosols can't be sent by Royal Mail. We appreciate your understanding.

Delivery of temperature controlled items

Some products, such as insulin and frozen food, need to be delivered in insulated packaging to prevent them from getting too warm (or too cold) during transit from us to you. Purchasing any of these items in your order will result in a £1.99 charge being added to the total to cover the high cost of the insulated packaging materials. You only pay the £1.99 once per order, regardless of how many temperature controlled items you purchase in that order.

How do I cancel or return an order?

Please call us as soon as possible if you need to amend or cancel an order on 01582 842096. If your order has been processed for dispatch we will be unable to cancel or amend the order. You will however be able to return your product for a full refund*.

To return an item, you must contact us by phone or email to arrange this BEFORE posting any product back to us. We will explain the process at this stage for you.

*For full details on returns, see our terms and conditions page.

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