Dentinox Infant Colic Drops
Methyl parahydroxybenzoate E218
Ethyl parahydroxybenzoate E214
Propyl parahydroxybenzoate E216
For all excipients, see 6.1
Translucent white liquid
For the gentle relief of wind and griping pains in infants, caused by the accumulation of ingested air. Facilitates eructation. Can be used from birth onwards.
2½ ml (one measured dose of the syringe) with or after each feed. May be added to the infant's bottle or given orally directly from the syringe. Maximum 6 doses per day. For infants can be used from birth onwards.
Hypersensitivity to the active substances or to any of the excipients
Contains sucrose. Patients with rare hereditary problems of fructose intolerance, glucose-galactose malabsorption or sucrase-isomaltase insufficiency should not take this medicine.
Keep all medicines out of the reach of children.
If symptoms persist obtain medical advice.
Levothyroxine may bind to simeticone. Absorption of levothyroxine may be impaired if Dentinox Infant Colic Drops are given concurrently to infants treated for thyroid disorders.
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.
From the literature it would appear that all the silicone will be excreted unchanged and that there was no increase of urinary silicate output or of absorption of the silicone.
It was concluded that the Activated Dimeticone carried no significant carcinogenic hazard, and that no other significant toxic effect attributable to Activated Dimeticone has been observed.
Overdosage may prove a problem with diabetics because of the sugar content.
Excessive swallowing of air results in collection of gas in the intestine. This can be the result of too rapid eating, excessive use of a pacifier (dummy), finger sucking or yelling. When the swallowed air is in the intestine, bubbles are formed, which makes it more difficult for the gas to pass through the intestine canal, resulting in abdominal distension and pain. Activated Dimeticone is a surface active substance which changes the surface tension of the intestinal mucus. Thus, the air bubbles burst and the gas is released. The elimination of the gas, air or foam from the gastro-intestinal tract, relieves abdominal distension and dyspepsia.
Activated Dimeticone is chemically inert and is not absorbed. Its effect is local on the intestinal contents.
No side effects from the substance are reported from the literature.
From the toxicity trials undertaken by Dow Corning, it has been demonstrated in the rat that all the Dimeticone was recovered in the faeces and that there was no increase in urinary salicate output.
In four human subjects given 376.5mg of Activated Dimeticone, twice daily for 10 days, it was found that there was no increase in their urinary silicate output and no evidence of absorption of the silicone.
There are no pre-clinical data of relevance to the prescriber which are additional to that already included in other sections of the SPC
Purified Water, Sucrose, Carbomer, Dill Oil, Sodium Hydroxide, Methyl parahydroxybenzoate E218, Ethyl parahydroxybenzoate E214, Propyl parahydroxybenzoate E216.
Do not store above 25 °C.
Pack size 100ml
100ml - HDPE round bottle with a jay cap tamper evident closure, with 2.5ml oral dosing syringe.
Pack size 2.5ml
40gsm craft paper, 10 gsm polyethylene, 8gsm aluminium foil and 30gsm surlyn.
Not all pack sizes may be marketed.
After use, rinse the syringe with warm water and dry. Not suitable for steam sterilisation.
Dendron Brands Limited
94, Rickmansworth Road
Watford, Hertfordshire, WD18 7JJ,
29th November 1976 / 09th September 2008