GOLDEN UDDER GEL
Land: Irland
Språk: engelsk
Kilde: HPRA (Health Products Regulatory Authority)
Preparatomtale
(SPC)
08-06-2024
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Aktiv ingrediens:
SULFUR, SALICYLIC ACID
Tilgjengelig fra:
Collective Chemical Company Ltd.
ATC-kode:
QD11AC08
INN (International Name):
SULFUR, SALICYLIC ACID
Dosering :
Per Cent
Legemiddelform:
Gel
Resept typen:
LM-Licensed Merchant
Terapeutisk gruppe:
Bovine
Terapeutisk område:
Sulfur compounds
Indikasjoner:
N.S.A.I.D
Autorisasjon status:
Authorised
Autorisasjon dato:
1993-03-12
Preparatomtale
IRISH MEDICINES BOARD ACT 1995
EUROPEAN COMMUNITIES (ANIMAL REMEDIES) (NO. 2) REGULATIONS 2007
(S.I. NO. 786 OF 2007)
VPA: 10914/001/001
Case No: 7004549
The Irish Medicines Board in exercise of the powers conferred on it by Animal Remedies (No. 2) Regulations (S.I. No. 786 of 2007) hereby
grants to:
COLLECTIVE CHEMICAL COMPANY LTD.
43 BIBURY AVENUE, STOKE LODGE, BS12 6DF, UNITED KINGDOM
an authorisation, subject to the provisions of the said Regulations and the general conditions of the attached authorisation, in respect of the
Veterinary Medicinal Product:
GOLDEN UDDER GEL
The particulars of which are set out in Part 1 and Part 2 of the said Schedule. The authorisation is also subject to any special conditions as may
be specified in the said Schedule.
The authorisation, unless previously revoked, shall continue in force from 11/03/2008.
Signed on behalf of the Irish Medicines Board
________________
A person authorised in that behalf by the said Board.
(NOTE: From this date of effect, this authorisation replaces any previous authorisation in respect of this product which is now null and void.)
IRISH MEDICINES BOARD
________________________________________________________________________________________________________________________
_Date Printed 22/08/2009_
_CRN 7004549_
_page number: 1_
PART II
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Golden Udder Gel
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Active substances
Sulphur for External Use
10.0 % w/w
Salicylic Acid
1.5 % w/w
For a full list of excipients see section 6.1.
3 PHARMACEUTICAL FORM
Gel. A yellow aqueous gel.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Bovine
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
An aid in the control of bovine mastitis.
For the treatment of minor skin conditions.
4.3
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