Chanatol Oral Solution

Land: Irland

Språk: engelsk

Kilde: HPRA (Health Products Regulatory Authority)

Aktiv ingrediens:

Cobalt sulphate heptahydrate; Propylene glycol

Tilgjengelig fra:

Chanelle Pharmaceuticals Manufacturing Limited

ATC-kode:

QA16QA

INN (International Name):

Cobalt sulphate heptahydrate; Propylene glycol

Dosering :

0.099, 99 percent weight/volume

Legemiddelform:

Oral solution

Resept typen:

LR: Licensed Retailer as defined in national legislation

Terapeutisk gruppe:

Cattle, Goats, Sheep

Terapeutisk område:

Drugs for prevention and/or treatment of acetonemia

Indikasjoner:

Vitamins and minerals

Autorisasjon status:

Authorised

Autorisasjon dato:

1991-10-01

Preparatomtale

SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Chanatol Oral Solution
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
3 PHARMACEUTICAL FORM
Oral solution.
A clear, light pink coloured solution.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Cattle, sheep and goats.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the treatment of acetonaemia in cattle and pregnancy toxaemia in
sheep and goats.
4.3 CONTRAINDICATIONS
Do not use in animals known to be hypersensitive to the active
substances.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None known.
4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTIONS FOR USE IN ANIMALS
None known.
SPECIAL PRECAUTIONS TO BE TAKEN BY THE PERSON ADMINISTERING THE
VETERINARY MEDICINAL PRODUCT TO ANIMALS
Wash splashes from the skin.
Each ml contains:
Active substances
Cobalt sulphate heptahydrate
0.099 % w/v
Propylene glycol
to 100
% w/v
For a full list of excipients, see section 6.1
I
R
I
S
H
M
E
D
I
C
I
N
E
S
B
O
A
R
D
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
___
_D_
_a_
_t_
_e_
_ _
_P_
_r_
_i_
_n_
_t_
_e_
_d_
_ _
_2_
_3_
_/_
_0_
_1_
_/_
_2_
_0_
_1_
_4_
_C_
_R_
_N_
_ _
_7_
_0_
_1_
_6_
_8_
_2_
_4_
_p_
_a_
_g_
_e_
_ _
_n_
_u_
_m_
_b_
_e_
_r_
_:_
_ _
_1_
4.6 ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS)
None known at the correct dosage.
4.7 USE DURING PREGNANCY, LACTATION OR LAY
The product may be used safely in pregnant and lactating animals.
4.8 INTERACTION WITH OTHER MEDICINAL PRODUCTS AND OTHER FORMS OF
INTERACTION
None known.
4.9 AMOUNTS TO BE ADMINISTERED AND ADMINISTRATION ROUTE
For oral administration only.
Shake well before use.
Cat