Skip to main content

PEROXYL MOUTHWASH

Active substance(s): HYDROGEN PEROXIDE

PDF Transcript

SUMMARY OF PRODUCT CHARACTERISTICS

1

NAME OF THE MEDICINAL PRODUCT
Peroxyl ™ Mouthwash.

2

QUALITATIVE AND QUANTITATIVE COMPOSITION

100ml of solution contains 1.5g of Hydrogen peroxide (as 30% Hydrogen
Peroxide solution).
For a full list of excipients, see section 6.1

3.

PHARMACEUTICAL FORM
Mouthwash
A clear aqua-blue liquid

4.

CLINICAL PARTICULARS

4.1.

Therapeutic Indications
As a cleanser in the symptomatic relief of minor mouth and gum irritations.

4.2

Posology and method of administration
Do not use in children under the age of 6.
Peroxyl is ready to use. Rinse with 10 ml (one capful, 10 ml line within cap) for
approximately one minute, then spit out. Use 3 times daily (after meals and at
bedtime) or as directed by a doctor or dentist.
Adults and children over 12 years: as above.
Children between 6 - 12 years old: Use under the supervision of an adult.
The duration of the treatment should not exceed 7 days.
Method of administration: Oromucosal use.

4.3.

Contraindications
This medicinal product must not be used in cases of hypersensitivity of the
active substance or to any of the excipients.

4.4.

Special warning and precautions for use
DO NOT SWALLOW.
If irritation persists for 7 days, is severe, is due to orthodontic appliances
and/or dentures, or swelling or fever develops, the patient's condition
needs to be re-evaluated by a doctor or dentist.
Overdose can injure the gums and continued use of hydrogen peroxide
may cause reversible hypertrophy of the papillae of the tongue known as
‘black hairy tongue’ therefore using this product at high doses or for long
periods of time is not recommended.
Avoid contact with eyes.

4.5

Interaction with other medicinal products and other forms of interaction
None known

4.6.

Pregnancy and Lactation
Although there are not sufficient specific clinical data on the use of Peroxyl in
this patient group, self-administration without medical advice is not
recommended.

4.7.

Effects on ability to drive and use machines
Not relevant

4.8

Undesirable effects

Some cases of mucosal irritation and swelling of the oral tissues have been reported
specially with high doses or in continued use (see special warnings, above). The
symptoms will resolve on stopping treatment with Peroxyl.
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
Yellow Card Scheme at: www.mhra.gov.uk/yellowcard.

4.9.

Overdose
Peroxyl is a dilute hydrogen peroxide solution and is unlikely to cause the
symptoms of overdosage associated with strong solutions (30-40%).
Peroxyl contains levo-menthol which if accidentally ingested at excessive
amounts may cause convulsions, particularly in infants and children.

5.

PHARMACOLOGICAL PROPERTIES

5.1.

Pharmacodynamic properties
Pharmacotherapeutic group: Antiinfectives and antiseptics for local oral
treatment
ATC code: A01AB02
Hydrogen peroxide is an oral antiseptic cleanser. The principal action is
brought about by contact of hydrogen peroxide with peroxidases and
catalases present in tissues and saliva, which causes the rapid release of
oxygen. This provides mechanical cleansing which flushes out mouth
debris, and helps in the treatment of oral irritations.

5.2.

Pharmacokinetic Properties
In the mouth, salivary peroxidase breaks down hydrogen peroxide to release
water and oxygen.

5.3.

Pre-clinical Safety Data
Low doses of hydrogen peroxide do not produce tissue damage or result in
neoplastic changes. Application of Peroxyl to abraded mucosa in the hamster
cheek pouch study over 21 days showed no adverse effect.

Hydrogen peroxide is not genotoxic in animals. The available data on
reproductive toxicology are incomplete but do not indicate an effect at low
concentrations.

6.

PHARMACEUTICAL PARTICULARS

6.1.

List of excipients
Purified Water
Sorbitol 70%w/w (non-crystallising)
Ethanol 96%
Poloxamer 388
Polysorbate 20
Methyl salicylate
Levo-Menthol
Sodium saccharin
Brilliant Blue FCF (E133)

6.2.

Incompatibilities
Not applicable.

6.3

Shelf life

24 months (300 ml pack size)

6.4.

Special Precautions for Storage
Do not store above 25°C.

6.5

Nature and contents of container

300 ml in bottle (PET), with polyethylene cap

6.6.

Special precautions for disposal
No special requirements

7.

MARKETING AUTHORISATION HOLDER
Colgate-Palmolive (UK) Ltd
Guildford Business Park
Middleton Road
Guildford
Surrey GU2 8JZ
UK

8.

MARKETING AUTHORISATION NUMBER(S)
PL 00049/0038

9

DATE OF FIRST AUTHORISATION/RENEWAL OF THE
AUTHORISATION
29/11/2006

10

DATE OF REVISION OF THE TEXT
17/02/2016

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.