Hydrogen Peroxide Solution (3%) Bp 10 Vols
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Hydrogen Peroxide Solution 3% BP 10 Vols
2. Qualitative and Quantitative Composition
Hydrogen peroxide aqueous solution 35% 7.5% v/v as the active ingredient. For a full list of excipients, see section 6.1.
3. Pharmaceutical Form Solution.
A clear, colourless solution.
4 CLINICAL PARTICULARS
4.1 Therapeutic indications
1. As a mild disinfectant for minor cuts, wounds and skin ulcers.
2. As a mouthwash or gargle.
4.2 Posology and method of administration
Topical.
Recommended dose and dosage schedule
1. As a disinfectant use as required. Dress the wound with cotton wool soaked in the peroxide.
2. As a mouthwash or gargle dilute one part of the peroxide to two parts of water (e.g. 5ml of peroxide and 10ml of water). Rinse the mouth for two to three minutes. This may be repeated up to three times daily.
As a disinfectant this product is suitable for use by adults, children and the elderly.
As a mouthwash or gargle the product is suitable for use by adults, children over 12 years and the elderly. Due to the risk of swallowing it should only be used by younger children under the instruction of a doctor.
4.3 Contraindications
Not for use in closed body cavities or on surgical wounds due to the risk of oxygen released into the circulation causing gas embolism.
Not for use as a disinfection agent for surgical instruments (particularly endoscopes) and as an enema.
4.4. Special warnings and special precautions for use
For external use only.
Keep all medicines away from children.
Not for use in closed body cavities or on surgical wounds due to risk of oxygen released into the circulation causing gas embolism.
Avoid normal skin.
Product bleaches fabric.
4.5. Interactions with other Medicaments and other forms of Interaction
None known.
4.6. Pregnancy and Lactation
All medicines should be avoided if possible during pregnancy and lactation. No evidence is available as to the safety of use of this product in these conditions.
4.7. Effects on Ability to Drive and Use Machines
None known.
4.8. Undesirable effects
Cases of gas embolism, sometimes resulting in cardiac arrest, have been reported when hydrogen peroxide has been instilled in closed body cavities or deep surgical wounds.
Strong solutions of hydrogen peroxide produce irritating burns on the skin and mucous membranes with a white eschar. The pain disappears after about 1 hour. Continued use of the product as a mouthwash may cause reversible hypertrophy of the papillae of the tongue.
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.
4.9 Overdose
Accidental ingestion may cause sore throat, gastric disturbances and vomiting. Sudden evolution of oxygen may cause injury by acute distension of the stomach and internal bleeding. Water may be given to drink. Ingestion of large volumes can lead to gas embolism following evolution of oxygen in the stomach.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic properties
A01A B02 - Antiinfectives and antiseptics for local oral treatment.
Hydrogen peroxide is used as a disinfectant and deodorant. It releases oxygen when applied to tissues, the effect lasts only as long as the oxygen is being released and is of short duration. The antimicrobial effect of the liberated oxygen is reduced in the presence of organic matter. It is used to cleanse wounds and ulcers in concentrations of up to 6%. Adhering and blood-soaked dressings may be released by the application of a solution of hydrogen peroxide. A l.5% solution has been used as a mouthwash in the treatment of acute stomatitis and as a deodorant gargle.
5.2. Pharmacokinetic Properties
No further information available.
5.3. Preclinical safety data
No data of relevance which is additional to that already included in other sections of the SPC.
6. PHARMACEUTICAL PARTICULARS
6.1. List of Excipients
Concentrated Phosphoric acid
Phenacetin
Purified water
6.2. Incompatibilities
Incompatible with reducing agents including organic matter and oxidisable substances and with alkalis, iodides, permanganates and other stronger oxidising agents. Its decomposition is increased by metallic salts, light, agitation, heat and metals.
6.3 Shelf life
36 months unopened.
6.4. Special Precautions for Storage
Do not store above 25°C. Store in the original container.
6.5 Nature and contents of container
200ml: Round amber glass bottle with white 28mm cap with tamper evident band and EPE Saranex liner.
6.6. Instruction for Use/Handling and Disposal
None.
7. MARKETING AUTHORISATION HOLDER
Thornton & Ross Limited Linthwaite Laboratories Huddersfield HD75QH
MARKETING AUTHORIZATION NUMBER(S)
8.
PL 00240/5106R
9 DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION
21/10/2008
10 DATE OF REVISION OF THE TEXT
11/05/2015