Aqueous cream

Land: Storbritannia

Språk: engelsk

Kilde: MHRA (Medicines & Healthcare Products Regulatory Agency)

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Last ned Preparatomtale (SPC)
04-09-2019

Aktiv ingrediens:

Emulsifying wax; White soft paraffin; Liquid paraffin; Phenoxyethanol; Purified water

Tilgjengelig fra:

Thornton & Ross Ltd

ATC-kode:

n/a

INN (International Name):

Emulsifying wax; White soft paraffin; Liquid paraffin; Phenoxyethanol; Purified water

Dosering :

90mg/1gram ; 150mg/1gram ; 60mg/1gram ; 10mg/1gram ; 690mg/1gram

Legemiddelform:

Cutaneous cream

Administreringsrute:

Cutaneous

Klasse:

No Controlled Drug Status

Resept typen:

Valid as a prescribable product

Produkt oppsummering:

BNF: 13020101; GTIN: 5011309026610

Preparatomtale

                                OBJECT 1
AQUEOUS CREAM BP
Summary of Product Characteristics Updated 12-Sep-2019 | Thornton &
Ross Ltd
•
1. Name of the medicinal product
•
2. Qualitative and quantitative composition
•
3. Pharmaceutical form
•
4. Clinical particulars
•
4.1 Therapeutic indications
•
4.2 Posology and method of administration
•
4.3 Contraindications
•
4.4 Special warnings and precautions for use
•
4.5 Interaction with other medicinal products and other forms of
interaction
•
4.6 Fertility, pregnancy and lactation
•
4.7 Effects on ability to drive and use machines
•
4.8 Undesirable effects
•
4.9 Overdose
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5. Pharmacological properties
•
5.1 Pharmacodynamic properties
•
5.2 Pharmacokinetic properties
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5.3 Preclinical safety data
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6. Pharmaceutical particulars
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6.1 List of excipients
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6.2 Incompatibilities
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6.3 Shelf life
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6.4 Special precautions for storage
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6.5 Nature and contents of container
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6.6 Special precautions for disposal and other handling
•
7. Marketing authorisation holder
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8. Marketing authorisation number(s)
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9. Date of first authorisation/renewal of the authorisation
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10. Date of revision of the text
1. Name of the medicinal product
Aqueous Cream BP
2. Qualitative and quantitative composition
Emulsifying ointment
30% w/w
White soft paraffin
15%w/w
Liquid paraffin
6.0%w/w
Excipient(s) with known effect
This product contains sodium lauryl sulfate 0.9%w/w, cetostearyl
alcohol 8.1%w/w and phenoxyethanol
1%w/w, see section 4.4.
For full list of excipients, see section 6.1.
3. Pharmaceutical form
Cream
4. Clinical particulars
4.1 Therapeutic indications
For the topical application to the skin:
As an emollient for the symptomatic relief of dry skin conditions.
As a soap-substitute for skin washing.
4.2 Posology and method of administration
_Adults, children and the elderly _
To be applied to the skin as required.
4.3 Contraindications
Contraindicated in patients with known hypersensitivity to
phenoxyethanol.
4.4 Special warnings and precautions for use
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