- 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
- 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
Bonjela Junior gel
2. Qualitative and quantitative composition
Lidocaine hydrochloride 0.5% w/wCetylpyridinium chloride 0.025% w/wFor a full list of excipients, see section 6.1.
3. Pharmaceutical form
4. Clinical particulars
4.1 Therapeutic indications
For the relief of pain from common mouth ulcers, denture irritation and infant teething pain.
4.2 Posology and method of administration
Route of Administration: Oromucosal
Adults, the elderly and children over 3 months:Apply a little gel to the sore area with either a clean finger tip or swab. This may be repeated after twenty minutes and then every three hours.
Known hypersensitivity to anaesthetics of the amide type. Hypersensitivity to any of the active ingredients or excipients. Babies under 3 months.
4.4 Special warnings and precautions for use
To be used with caution in patients with hepatic or cardiac dysfunction.Do not exceed the stated dose. Not recommended for infants under three months. Keep out of the reach and sight of children. If symptoms persist consult your doctor or dentist.
4.5 Interaction with other medicinal products and other forms of interaction
Concurrent use of either cimetidine or propranolol increases the risk of lidocaine toxicity. Lidocaine is antagonised by those diuretics which cause hypokalaemia.
4.6 Fertility, pregnancy and lactation
Pregnancy:The safety of the product for use in human pregnancy has not been established. The product is, therefore, not recommended during pregnancy.Lactation/Breastfeeding:Lidocaine is distributed into breast milk, but in such small quantities that there is generally no risk of the child being affected at therapeutic dose levels. No adverse effects have been seen in breast-fed infants whose mothers were receiving lidocaine and it is therefore usually compatible with breast feeding.Fertility:No data on human fertility are available.
4.7 Effects on ability to drive and use machines
4.8 Undesirable effects
Adverse reactions have been ranked under headings of frequency using the following convention:Very common: ≥ 1/10Common: ≥ 1/100 to < 1/10Uncommon: ≥ 1/1,000 to < 1/100Rare: ≥ 1/10,000 to <1/1,000Very Rare: < 1/10,000Not known: Frequency unable to be classified from available data.Within each frequency grouping, undesirable effects are presented in order of decreasing seriousness.
|System Organ Class||Preferred Term||Frequency|
|Blood and lymphatic system disorders||Methaemoglobinaemia||Not known|
|Immune System Disorders||Hypersensitivity||Not known|
|Skin and subcutaneous tissue disorders||Contact dermatitis||Not known|
Overdose is highly unlikely given the size of the pack. No experience of overdosage.It is most unlikely, even with misuse or excessive application of the gel, that the large amounts of lidocaine hydrochloride or cetylpyridinium chloride required to produce clinically-relevant toxic effects would be reached. In the event of overdose, use should be discontinued and a doctor consulted.The toxic effects of lidocaine are directly related to blood concentrations. Symptoms are dizziness, cyanosis due to methaemoglobinaemia, fall of blood pressure, muscular tremors, convulsions, coma, irregular and weak breathing, cardiac standstill and bronchial spasm. Removal of the ingested drug by induced emesis followed by activated charcoal is only useful if the patient is seen within 30 minutes of ingestion. The airway must be maintained and artificial respiration with oxygen given until convulsions or depression are controlled and blood pressure and pulse return to normal.Convulsions can be controlled with diazepam (0.1 mg/kg i.v.) or succinylcholine chloride (10-50 mg i.v. slowly). Perform artificial respiration with oxygen until convulsions are controlled and continue giving oxygen until blood pressure and pulse return to normal. Adequate arterial oxygen saturation must be maintained. If convulsions are not continuous the administration of oxygen may be sufficient to maintain the patient until the blood level of lidocaine falls. Do not give stimulants. The methaemoglobinaemia can be treated by methylene blue (1%, 0.1 ml/kg, i.v. over ten minutes). Treat fall in blood pressure by postural means (head down, feet raised, supine position) or with i.v. saline or blood transfusion if shock threatens. The critical period does not exceed one hour.Suppression of pharyngeal sensation with concomitant effects on swallowing may theoretically result from excessive topical oral use of the gel. Such an effect has been reported in an adult who gargled and swallowed 5 ml of a 2% lidocaine hydrochloride solution (equivalent to 100 mg of lidocaine). However, assuming proportionality of body surface area and pharyngeal surface area, this dose would be equivalent to a single dose of 3.6 g of the gel for a three month old child.
5. Pharmacological properties
5.1 Pharmacodynamic properties
Local anaesthetic /analgesic - antiseptic.
5.2 Pharmacokinetic properties
5.3 Preclinical safety data
There are no pre-clinical data of relevance to the prescriber which are additional to that already included in other sections of the SPC.
6. Pharmaceutical particulars
6.1 List of excipients
Ethanol 96% Glycerol Banana Flavour (contains Propylene glycol)Sodium SaccharinCarbomerTriethanolamineWater
6.3 Shelf life
6.4 Special precautions for storage
Do not store above 25°C.
6.5 Nature and contents of container
10g of product is filled into a 16 x 101mm aluminium collapsible tube internally lacquered with a 9mm membrane nozzle with spiked cap. 15g of product is filled into an aluminium collapsible tube, internally lacquered, with an aluminium membrane at the nozzle, sealed with latex, fitted with a white polyethylene flower pot cap. The tube is then packed into a carton.Not all pack sizes may be marketed.
6.6 Special precautions for disposal and other handling
7. Marketing authorisation holder
Reckitt Benckiser Healthcare UK Limited,Wellcroft House, Wellcroft Road,Slough,SL1 4AQUnited Kingdom
8. Marketing authorisation number(s)
9. Date of first authorisation/renewal of the authorisation
22 January 1988 / 04 Feburary 2000
10. Date of revision of the text
Reckitt Benckiser Healthcare (UK) Ltd
RB Consumer Relations, PO Box 4644, SLOUGH, SL1 0NS, UK
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