Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations, 2000

JurisdictionIreland
Year2000
CitationIR SI 116/2000

I, Micheal Martin, Minister for Health and Children, in exercise of the powers conferred on me by section 32 of the Irish Medicines Board Act, 1995 (No. 29 of 1995), as adapted by the Health (Alteration of Name of Department and Title of Minister) Order, 1997 ( S.I. No. 308 of 1997 ), hereby make the following Regulations-

1. These Regulations may be cited as the Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations, 2000.

2. These Regulations shall be construed as one with the Medicinal Products (Prescription and Control of Supply) Regulations, 1996 to 1999 and may be cited together with those Regulations as the Medicinal Products (Prescription and Control of Supply) Regulations, 1996 to 2000.

3. The Medicinal Products (Prescription and Control of Supply) Regulations, 1996 ( S.I. No. 256 of 1996 ), as amended by the Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations, 1996 ( S.I. No. 309 of 1996 ) and by the Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations, 1999 ( S.I. No. 271 of 1999 ), are hereby amended by the substitution in the First Schedule thereto, for the entries in Columns 2, 3, 4 and 5 in respect of the substance specified in Column 1 of the Schedule to these Regulations, of the entries in Columns 2, 3, 4 and 5 of the Schedule to these Regulations.

Schedule

Substances which when contained in medicinal products are subject to prescription control and circumstances excluding certain products from such control

Circumstances excluding medicinal products from prescription control

Column

Column

Column

Column

Column

1

2

3

4

5

Substance

Part in Schedule

Maximum strength, pack size or period of treatment

Use, pharmaceutical form or manner of administration

Maximum dose and maximum daily dose

Hydrocortisone acetate

A

(1) Equivalent to 1.0% of Hydrocortisone (MS)

(1) External:

For use in irritant dermatitis, contact allergic dermatitis, insect bite reactions and mild to moderate eczema.

15.0g (MPS)

For use in adults and children not under 10 years.

(2) Equivalent to 1.0% of Hydrocortisone (MS)

15.0g (MPS)

(2) External:

In ointments when in combination with one or more of the following: Benzyl Benzoate, Bismuth Oxide, Bismuth Subgalate, Peru Balsam, Pramoxine Hydrochloride...

To continue reading

Request your trial

VLEX uses login cookies to provide you with a better browsing experience. If you click on 'Accept' or continue browsing this site we consider that you accept our cookie policy. ACCEPT