Golden Udder Gel

Country: United Kingdom

Language: English

Source: VMD (Veterinary Medicines Directorate)

Active ingredient:

Salicylic Acid, Sulphur

Available from:

Mr J J & Mrs M A Zakarias

ATC code:

QD11AC08

INN (International Name):

Salicylic Acid, Sulphur

Pharmaceutical form:

Gel

Prescription type:

AVM-GSL - Authorised Veterinary Medicine – General Sales List

Therapeutic group:

Cattle

Therapeutic area:

Antiseptic

Authorization status:

Authorized

Authorization date:

2002-04-06

Summary of Product characteristics

Revised: 15 January 2009
AN: 01321/2008
SUMMARY OF PRODUCTS CHARACTERISTICS
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Golden Udder Gel
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Qualitative composition
Active Substances
Sulphur for external use
Salicylic Acid
For full list of excipients, see
section 6.1
Quantitative composition
% w/w
10.0
1.5
3.
PHARMACEUTICAL FORM
Gel;
Yellow aqueous gel
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Cattle
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
a) An aid in the control of bovine mastitis
b) A soothing antiseptic gel for cattle the treatment of minor skin
conditions
4.3
CONTRAINDICATIONS
None known.
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
Topical application only.
Revised: 15 January 2009
AN: 01321/2008
4.5
SPECIAL PRECAUTIONS FOR USE
I.
SPECIAL PRECAUTIONS FOR USE IN ANIMALS
Wash and dry udders and teats before milking
If symptoms of mastitis persist after 6 days consult your
veterinary surgeon
For external use only
II.
SPECIAL PRECAUTIONS FOR THE PERSON ADMINISTERING THE
VETERINARY MEDICINAL PRODUCT TO ANIMALS
Avoid contact with eyes. In the event of accidental eye contact,
rinse with plenty of clean water and seek medical advice. In the
event of accidental ingestion wash out mouth thoroughly with
water, then drink plenty of water and seek medical advice. Wash
hands after use. The use of a barrier cream is recommended
should dryness of the hands occur.
4.6
ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS)
None known
4.7
USE DURING PREGNANCY, LACTATION OR LAY
The product may be used in pregnant and lactating cows.
4.8
INTERACTION WITH OTHER MEDICINAL PRODUCTS AND OTHER FORMS OF
INTERACTION
a) With other medicinal products: None known
b) Other interactions: None known
4.9
AMOUNT(S) TO BE ADMINISTERED AND ADMINISTRATION ROUTE
_1. CLINICAL MASTITIS:_
At each milking rub in sufficient product to cover the infected
quarter
(approximately
20
-
30
g
-
up
to
1
level
tablespoon).
Continue
treatment for a minimum of three days. If symptoms persist after 6
days consult you