Simple Linctus Sugar Free
Active ingredient: citric acid monohydrate
- 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 Pregnancy and lactation
- 4.7 Effects on ability to drive and use machines
- 4.8 Undesirable effects
- 4.9 Overdose
- 5. Pharmacological properties
- 5.1 Pharmacodynamic properties
- 5.2 Pharmacokinetic properties
- 5.3 Preclinical safety data
- 6. Pharmaceutical particulars
- 6.1 List of excipients
- 6.2 Incompatibilities
- 6.3 Shelf life
- 6.4 Special precautions for storage
- 6.5 Nature and contents of container
- 6.6 Special precautions for disposal and other handling
- 7. Marketing authorisation holder
- 8. Marketing authorisation number(s)
- 9. Date of first authorisation/renewal of the authorisation
- 10. Date of revision of the text
1. Name of the medicinal product
Simple Linctus Sugar Free
2. Qualitative and quantitative composition
Simple Linctus Sugar Free: Citric Acid Monohydrate 125 mg/5 ml equivalent to 114.29mg/5ml Anhydrous Citric Acid.
3. Pharmaceutical form
Clear Sugar Free Syrup
4. Clinical particulars
4.1 Therapeutic indications
For the management of a mild non-specific cough.
4.2 Posology and method of administration
Adults: One 5 ml spoonful orally 3-4 times daily.
Children: Not appropriate
4.3 Contraindications
Not known
4.4 Special warnings and precautions for use
This medicine contains maltitol liquid. Patients with rare hereditary problems of fructose intolerance should not take this medicine.
This medicinal product contains small amounts of ethanol (alcohol), less than 100mg per 5ml dose
4.5 Interaction with other medicinal products and other forms of interaction
None Known
4.6 Pregnancy and lactation
No data available
4.7 Effects on ability to drive and use machines
Not applicable
4.8 Undesirable effects
Immune system disorders:Not Known: Hypersensitivity reactions including facial oedema (mainly swollen lips and/or mouth) and rash have been reported.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
4.9 Overdose
Sufficient prolonged overdose of citric acid may cause erosion of the teeth and have a local irritant action.
5. Pharmacological properties
5.1 Pharmacodynamic properties
Absorption: Citric Acid Monohydrate is absorbed after oral administration.
Distribution: Citric Acid is found naturally in the body and is widely distributed, about 70% of the citric acid in the body is in hard bone and this accounts for 1.5% of bone content.
Metabolic Reactions: It is an important intermediate in carbohydrate metabolism and its major role is in the tricarboxylic acid cycle (Krebs citric acid cycle); it is metabolised to carbon dioxide and water.
Excretion: Citric acid is normally excreted in the urine in amounts ranging from 0.4 to 1.5g daily and this amount is not increased unless very large doses are administered. The urinary excretion of citric acid is increased in alkaline urine
5.2 Pharmacokinetic properties
Not applicable
5.3 Preclinical safety data
None stated
6. Pharmaceutical particulars
6.1 List of excipients
Glycerol (E422)
Sodium Carboxymethylcellulose
Sodium Benzoate (E211)
Saccharin Sodium (E954)
Maltitol liquid (E965)
Ethanol (96%)
Star Anise Oil
Purified Water
6.2 Incompatibilities
Not appropriate
6.3 Shelf life
2 years
6.4 Special precautions for storage
Do not Store above 25°C.
6.5 Nature and contents of container
Amber glass bottles with pilfer screw closure
High density Polyethylene with screw on closure
Pack sizes of 100ml, 125ml, and 200ml for Amber Glass Bottles
Pack size of 2000ml for High Density Polyethylene dispensary pack.
6.6 Special precautions for disposal and other handling
As with all medicines.
7. Marketing authorisation holder
Pinewood Laboratories Limited
Ballymacarbry
Clonmel
Co Tipperary
8. Marketing authorisation number
PL 04917/0006
9. Date of first authorisation/renewal of the authorisation
28 August 1991
10. Date of revision of the text
12 September 2019