Dentinox Infant Colic Drops

Activated Dimeticone 42.00 mg/5ml

For excipients, see 6.1

Oral suspension

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.

None known..

Not applicable.

Not applicable.

None known.

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 , Nipasept [Methylhydroxybenzoate, Ethylhydroxybenzoate, Propylhydroxybenzoate].

None known.

2 years

Do not store above 25 ºC.

Pack size 100ml

100ml - HDPE round bottle with a jay cap tamper evident closure, with 2.5ml oral dosing syringe.

Pack size 2.5ml

Sample sachets:

40gsm craft paper, 10 gsm polyethylene, 8gsm aluminium foil and 30gsm surlyn.

After use, rinse the syringe with warm water and dry.

ADMINISTRATION DETAILS

DDD Limited,

94, Rickmansworth Road

Watford

Hertfordshire, WD18 7JJ.

PL 0133/0022

Date of first authorisation: 29^th November 1976

Date of last renewal: 9^th September 2008

July 2009