Kenostart Spray en Dip 3 mg/g Cutaneous spray, solution@Dip solution
Kenostart Spray en Dip 3 mg/g Cutaneous spray, solution@Dip solution
Authorised
- Iodine
Product identification
Medicine name:
Kenostart Spray en Dip 3 mg/g Cutaneous spray, solution@Dip solution
KENOSTART SPRAY E IMMERSIONE 3 mg/g Soluzione spray o per l’immersione dei capezzoli di bovini da latte
Active substance:
- Iodine
Target species:
-
Cattle
Route of administration:
-
Dipping
-
Nebulisation use
Product details
Active substance and strength:
-
Iodine3.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Teat dip/spray solution
Withdrawal period by route of administration:
-
Dipping
- Cattle
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 days
-
-
Nebulisation use
- Cattle
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD08AG03
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Available in:
-
Italy
Package description:
- Kenostart Spray en Dip 3 mg/g dip sol./cut. spray sol. 200 l
- Kenostart Spray en Dip 3 mg/g dip sol./cut. spray sol. 60 l
- Kenostart Spray en Dip 3 mg/g dip sol./cut. spray sol. 25 l
- Kenostart Spray en Dip 3 mg/g dip sol./cut. spray sol. 20 l
- Kenostart Spray en Dip 3 mg/g dip sol./cut. spray sol. 10 l
- Kenostart Spray en Dip 3 mg/g dip sol./cut. spray sol. 5 l
- Kenostart Spray en Dip 3 mg/g dip sol./cut. spray sol. 1 l
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Cid Lines
Marketing authorisation date:
Manufacturing sites for batch release:
- Cid Lines
Responsible authority:
- Ministry Of Health
Authorisation number:
- 103950
Date of authorisation status change:
Reference member state:
-
Belgium
Procedure number:
- BE/V/0042/001
Concerned member states:
-
Austria
-
Cyprus
-
Estonia
-
France
-
Germany
-
Greece
-
Ireland
-
Italy
-
Netherlands
-
Poland
-
Portugal
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 1/02/2023
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