Bovidip 20 mg/ml Concentrate for Teat Dip or Spray Solution

Available Iodine

Last verified

Veterinary medicinal product: teat dip/spray solution. Distribution category: AVM-GSL (Veterinary Medicines Regulations 2013, Schedule 3). Active substance: Available Iodine.1

In short: questions and answers

Does Bovidip 20 mg/ml Concentrate for Teat Dip or Spray Solution need a prescription?
Over the counter. As stated in the registration decision.1
Which animals is Bovidip 20 mg/ml Concentrate for Teat Dip or Spray Solution for?
Cattle.1
What is the active substance in Bovidip 20 mg/ml Concentrate for Teat Dip or Spray Solution?
Available Iodine. ATCvet code: QG52A.13
What is the withdrawal period of Bovidip 20 mg/ml Concentrate for Teat Dip or Spray Solution according to the leaflet?
Cattle, meat: 0 days; Cattle, milk: 0 days.3
Dispensing
Over the counter1

AVM-GSL: Authorised Veterinary Medicine - General Sale List. No prescription is needed and it may be sold by any retailer.12

Supplied without a prescription. As stated in the registration decision.

Animal species
Cattle1
Active substance
Available Iodine
ATCvet code
QG52A3
Manufacturer
Marketing authorisation holder: DeLaval NV

Withdrawal period

Animal speciesProductdays
Cattlemeat03
Cattlemilk03
Summary of product characteristics

Composition

Active substance:

2 g per 100 ml as available iodine (concentrate).

25 mg per 5 ml dose as available iodine (ready-to-use solution).

Excipients:

Qualitative composition of excipients and other constituentsQuantitative composition if that information is essential for proper administration of the veterinary medicinal product
Water Purified
Glycerol100 mg/ml
Macrogol lauryl ether
Poloxamer
Sodium iodide
Citric acid monohydrate
Sodium hydroxide

Clear Brown Liquid.

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Pharmacological properties

4.1 ATCvet code:

QG52A

4.2 Pharmacodynamics

Iodine solutions react with the organic matter of bacteria and viruses to render them harmless. The mechanism of kill appears to be due to an oxidative-reductive reaction, involving various cell wall constituents, which are irreversibly transformed. The sulfhydryl linkages, in bacterial cell wall components, are specifically targeted by iodine.

The veterinary medicinal product is bactericidal (EN 1040 and EN 1656) against:

Pseudomonas aeruginosa

Staphylococcus aureus

Enterococcus hirae

Proteus vulgaris

4.3 Pharmacokinetics

Literature suggests that absorption of iodine through the skin is well below levels which would lead to pharmacokinetic activity in the body.

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Target species

Cattle (dairy cattle)

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Indications

Teat disinfection as an aid in the prevention of mastitis.

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Dosage

Dilute before use. Prepare a fresh solution daily. Dilute one part of the veterinary medicinal product with three parts of clean water and mix well. Al-ways clean the dip cup or spray container after use. Amounts to be administered: about 5 ml of the diluted product per cow per application.

Administration route:

• Dipping: Dip each teat immediately after milking in a teat dip cup containing diluted product. Dip the full length of the teats and replenish the dip cup as necessary.

• Spraying: Spray the entire surface of the teats after each milking.

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Contraindications

Do not use in cases of hypersensitivity to the active substance or to any of the excipients.

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Adverse reactions

None known.

Reporting adverse events is important. It allows continuous safety monitoring of a veterinary medicinal product. Reports should be sent, preferably via a veterinarian, to either the marketing authorisation holder or the national competent authority via the national reporting system. See the label for respective contact details.

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Warnings

Special precautions for safe use in the target species:

For external use only. Allow product to dry before exposing the cows to wet (rainy), cold or windy conditions. Use on injured teats may delay the wound-healing process. It is recommended that treatment be discontinued until teat lesions have resolved. If signs of disease persist or appear, consult a veterinary surgeon.

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

Care should be taken to avoid eye contact. In case of eye contact, flush the eyes with copious amounts of water and seek medical advice. In case of accidental ingestion, seek medical advice immediately and show the combined package leaflet and label to the physician. When used as spray, avoid working in spray mist. Wash hands after use. Persons with io-dine allergy should wear gloves and mask. The use of gloves during milking and dipping or spraying is recommended to protect the skin and for hygienic milk collection.

Special precautions for the protection of the environment:

Not applicable.

3.11 Special restrictions for use and special conditions for use, including restrictions on the use of antimicrobial and antiparasitic veterinary medicinal products in order to limit the risk of development of resistance

Not applicable.

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Use during pregnancy, lactation or lay

Pregnancy and lactation:

Can be used during pregnancy and lactation.

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Interactions

The use of this product in the specified manner (topical antiseptic) has no known interactions with other medicaments or nutrition.

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Overdose

Not applicable. The product is for topical application. Significant absorption does not occur.

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Special warnings

Do not mix with other chemicals. Prior to milking, wash teats with an udder wash solution and dry with a disposable paper towel. Discard any product that becomes contaminated. Always use a clean spray or dip cup and clean after use.

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Withdrawal period

Meat and offal: Zero days.

Milk: Zero hours.

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Incompatibilities

In the absence of compatibility studies, this veterinary medicinal product must not be mixed with other veterinary medicinal products.

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Immediate packaging

High-density polyethylene 5, 10, 20, 60 or 200 litre cans closed with high-density polyethylene screw caps, secured with a sealing ring. Not all pack sizes may be marketed.

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Storage

Store upright in the tightly closed original container. Do not store above 25°C. Protect from frost. If the product has frozen, thaw in a warm place and shake well before use. For the larger pack sizes, the product should be rolled sufficiently to mix the solution. Under no circum-stances should an attempt be made to shake the 60 or 200 litre packs. Protect from light.

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Shelf life

Shelf life of the veterinary medicinal product as packaged for sale: 18 months

Shelf life after first opening the immediate packaging: 6 months

Shelf life after dilution according to directions: 1 day.

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Disposal of unused product

Medicines should not be disposed of via wastewater or household waste.

The veterinary medicinal should not enter water courses as iodine may be dangerous for fish and other aquatic organisms.

Use take-back schemes for the disposal of any unused veterinary medicinal product or waste materials derived thereof in accordance with local requirements and with any national collection systems applicable to the product concerned.

The 200-litre container should not be returned for re-filling.

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Additional information

Vm 17140/4008

8 DATE OF FIRST AUTHORISATION

09 July 2007

9 DATE OF THE LAST REVISION OF THE SUMMARY OF THE PRODUCT CHARACTERISTICS

June 2025

10 CLASSIFICATION OF VETERINARY MEDICINAL PRODUCT

Veterinary medicinal product not subject to prescription.

Find more product information by searching for the ‘Product Information Database’ on www.gov.uk.

Gavin Hall Approved: 22 August 2025

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Registration holder

DeLaval NV

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Regulations

Sources

  1. VMD Product Information Database: Bovidip 20 mg/ml Concentrate for Teat Dip or Spray Solution, 17140/4008 UK Veterinary Medicines Directorate (OGL v3.0), checked 2026-10-04 archived copy from 2026-10-04
  2. The Veterinary Medicines Regulations 2013, Schedule 3 (categories of veterinary medicinal products) UK Government, legislation.gov.uk, checked 2026-10-04 archived copy from 2026-10-04
  3. Summary of Product Characteristics: Bovidip 20 mg/ml Concentrate for Teat Dip or Spray Solution UK Veterinary Medicines Directorate, SPC of the marketing authorisation holder, checked 2026-10-04 archived copy from 2026-10-04