Hedrin® 4% cutaneous solution
Packaging to state: Hedrin 4% lotion dimeticone
For a full list of excipients, see section 6.1
Hedrin is a clear, colourless liquid
Hedrin is indicated for the eradication of headlice infestations
Adults and children (aged six months and above)
For topical external use only
Apply sufficient lotion to cover dry hair from the base to the tip to ensure that no part of the scalp is left uncovered. Work into the hair spreading the liquid evenly from roots to tips. Allow hair to dry naturally. Hedrin should be left on hair for a minimum of 8 hours or overnight. Wash out with normal shampoo, rinsing thoroughly with water. Repeat the treatment after seven days.
Children under the age of six months should only be treated under medical supervision.
Hypersensitivity to any of the ingredients
Discontinue at the first appearance of a skin rash or any other signs of local or general hypersensitivity. Should any signs of hypersensitivity occur (e.g. rashes, urticaria, generalised pruritus, breathing difficulties), the product should be shampooed off immediately, and if symptoms do not resolve, medical advice sought.
For external use only.
Avoid contact with the eyes but if accidentally introduced into the eyes, flush with water.
Hedrin 4% cutaneous solution is combustible when on the hair and in direct contact with an open flame or other source of ignition; therefore during treatment hair should be kept away from open flames or other sources of ignition.
The labels and leaflets will state:
Keep hair away from sources of ignition, especially naked flames and burning cigarettes, whilst being treated with Hedrin®. Treated hair can readily burn if ignited”.
Dimeticone is not known to interact with other drugs
There is no data to suggest that Hedrin may not be used in pregnancy.
Dimeticone is usually well tolerated.
Minor adverse events include skin irritation, an itchy or flaky scalp and irritation around the eyes.
Single cases of hair loss have been reported.
Signs of hypersensitivity reactions including rash, urticaria, generalised pruritus, and breathing difficulties.
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 at: www.mhra.gov.uk/yellowcard.
There are no known recognised symptoms of overdose.
It is unlikely that Hedrin will enter the bloodstream via scratched skin however if this does occur, available data suggests it will be rapidly eliminated unchanged. If the lotion were to be accidentally ingested, again, the available data suggests that there are no specific safety concerns.
No special procedures are likely to be needed.
The solution contains dimeticone, which is used in many pharmaceutical and cosmetic preparations. A 4% concentration has been found to affect the physico-physiological activity of lice. It is less effective in its ovicidal activity and therefore two applications 7 days apart are required.
Hedrin contains no neurotoxic organophosphate insecticides and therefore does not work by acting on specific enzymes within the louse. The Hedrin solution acts on the lice by a physical process to cover the lice and disrupt the ability of the lice to manage its water balance so that treated insects fail to excrete surplus water. Hedrin activity is not diminished in insecticide resistant head lice.
Hedrin is applied topically to the affected area but there is little or no absorption of Hedrin through the skin.
There are no further relevant data
Three years, when stored unopened
This product does not require any special storage conditions
HDPE dropper containers with screw caps; 150ml.
HDPE containers incorporating plastic trigger spray, cap and PE dip tube; 120ml capacity
Not all packs may be marketed
Care should be taken as the product may cause a slip hazard if accidentally spilt onto smooth surfaces
Thornton & Ross Ltd