DETTOL MED 0.20% W/W CUTANEOUS SPRAY SOLUTION - summary of medicine characteristics

1 NAME OF THE MEDICINAL PRODUCT

Dettol Med 0.20%w/w Cutaneous Spray solution

2 QUALITATIVE AND QUANTITATIVE COMPOSITION

Benzalkonium Chloride 0.20%w/w

Excipients with known effect: propylene glycol (E1520) Ph Eur 2.080% w/w

Fragrance containing allergens (in Mild Pine Fragrance)

For the list of excipients, see Section 6.1

Cutaneous Spray, Solution (Topical Spray)

Product is a clear colourless liquid with slight pine odour

4.1 Therapeutic indications

For the antiseptic cleansing of minor wounds

4.2 Posology and method of administration

For Cutaneous use

For adults and children over 12 months of age: For occasional, localised, shortterm use only. To be applied to fresh minor wounds to eliminate common bacteria associated with infection of minor wounds. The product should be sprayed to cover the entire wound and can be re-applied if the wound is reopened

For adults and children over 6 years of age: Spray a full dose (1 to 2 sprays) once onto each wound and leave for five minutes. If necessary use a clean tissue or cotton wool to wipe up any excess liquid.

For children aged between 1 and 6 years of age: Please seek the advice of a pharmacist or healthcare professional prior to use if you have any concerns. Spray once (1 spray) onto each wound (can only be applied to a maximum of 4 wounds at a time) and leave for five minutes. If necessary use a clean tissue or cotton wool to wipe up any excess liquid.

This medicinal product is for use once in 24 hours and for a maximum of 3 – 5 days. It should not be used on a continuous basis.

If you have concerns about your symptoms or your symptoms get worse, please contact a healthcare professional

The product is not intended to improve wound healing or be used to improve wound healing

4.3 Contraindications

Do not use on children of 1 years of age or under.

People with known hypersensitivity to Benzalkonium chloride or any of the excipients should not use Dettol Med Cutaneous spray

4.4 Special warnings and precautions for use

Label Warning: For external use only. Do not use around the eyes or genitalia or ears, in the mouth or over large areas of the body that exceed 5% of the total body surface area (5% is estimated to reflect minor wounds of both knees and elbows). Do not inhale. In the case of accidental eye contact, the eye should be irrigated with copious amounts of cold water.

This medicinal product contains propylene glycol and may cause skin irritation

This medicine contains Mild Pine fragrance containing D-Limonene and Lilial. D-Limonene and Lilial may cause allergic reactions.

Benzalkonium chloride may be deactivated when used with soap or any other surfactants.

4.5 Interaction with other medicinal products and other forms of interaction No specific drug interaction studies have been undertaken; therefore, we cannot recommend the use of Dettol Med Cutaneous Spray Solution with any other topical products.

4.6 Pregnancy and lactation

For Benzalkonium Chloride no clinical data on exposed pregnancies are available. Animal studies do not indicate direct or indirect harmful effects with respect to pregnancy, embryonal/foetal development, parturition or postnatal development. The potential risk for humans is unknown.

Use during pregnancy and lactation is not expected to be associated with harmful effects as cutaneous absorption is minimal. In order to avoid ingestion by a breast fed child, application to the breasts during lactation is not advised

4.7 Effects on ability to drive and use machines

Dettol Med Cutaneous Spray Solution has no influence on the ability to drive and use machines.

4.8 Undesirable effects

Post-marketing experience shows no adverse experiences specific to the topical application of Dettol Med Cutaneous Spray Solution; adverse experiences have been limited to those that are typically reported for topical antiseptics. Additional effects may occur. In general, the adverse reactions rate for topical antiseptics is very rare (<1/10,000).

Skin and subcutaneous tissue disorders:

Very Rare: skin dystrophy, acrodermatitis, exacerbation of eczema, contact dermatitis, alopecia or rash.

General disorders and administration site disorders:

Very Rare: (< 1/10,000) signs and symptoms of systemic allergic reactions, including papular rash, pruritus or rash.

Very Rare: local site reactions including application site fissure, a, skin irritation, skin burning sensation, erythema, skin discoloration or skin exfoliation

4.9 Overdose

Due to Benzalkonium Chloride low absorption into the systemic circulation following both oral and cutaneous application, its acute toxicity is very low and it is unlikely that any toxic effects would be seen in humans following either cutaneous dosing with Dettol Med Wound Spray as recommended or accidental ingestion. If necessary use a clean tissue or cotton wool to wipe up any excess liquid.

5 PHARMACOLOGICAL PROPERTIES

5.1 Pharmacodynamic properties

ATC Code: D08 AJ01 Group: Antiseptics and Disinfectants. Quaternary ammonium compounds.

Benzalkonium chloride is a quaternary ammonium compound which has been used for many years as a surfactant and antiseptic/di­sinfectant. It is known to be bactericidal in low concentrations (typically between 0.1 and 0.2%) to a wide range of Gram-positive and Gram-negative bacteria.

Benzalkonium chloride kills (a log 5 reduction) Staphylococcus aureus and beta-hemolytic Streptococci (e.g., Streptococcus pyogenes) in 1 minute, and Pseudomonas aeruginosa in 5 minutes

Note: EN 1276 is designed to evaluate the antimicrobial efficacy of disinfectant products intended for use in food, industrial, domestic and institutional areas. It can be used to assess efficacy. A Five log reduction of all organisms in 5 minutes is required to pass the EN1276.

5.2 Pharmacokinetic properties

Quaternary ammonium compounds such as Benzalkonium chloride are only absorbed to a very small extent through human skin.

5.3 Preclinical safety data

The low level of Benzalkonium chloride in the product, coupled with its low level of absorption from intact and broken skin, make it unlikely that any significant systemic toxic effects would arise from its use. There is evidence that it can have an irritant effect on mucous membranes.

6 PHARMACEUTICAL PARTICULARS

6.1 List of excipients

Propylene glycol

Sodium dihydrogen phosphate dihydrate

Disodium hydrogen phosphate dodecahydrate

Mild Pine fragrance

Disodium edetate, dihydrate

Purified water

6.2 Incompatibilities

Not applicable

6.3 Shelf life

10ml PolyPropylene bottle has a shelf life of 2 years.

100ml HDPE bottle has a shelf life of 3 years.

6.4 Special precautions for storage

No special storage conditions

6.5 Nature and contents of container

Polypropylene container, spray pump, with a polypropylene co-polymer overcap packed into polyethylene terephthalate (PET) blister and carton envelope.

The pack size is 10 ml.

HDPE container, spray pump, with a polypropylene co-polymer overcap.

The pack size is 100 ml.

Not all pack sizes may be marketed.