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GlaxoSmithKline UK

Stockley Park West, Uxbridge, Middlesex, UB11 1BT
Telephone: +44 (0)800 221 441
Fax: +44 (0)208 990 4328
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Summary of Product Characteristics last updated on the eMC: 23/11/2012
SPC Otosporin Ear Drops
Discontinued icon
Discontinued Items:
The preparation being discontinued is:
  • Otosporin ear drops (GlaxoSmithKline UK Ltd)
The pharmaceutical company has decided to discontinue this product and so it may not be available in the future. This document has been left on the eMC for information purposes.

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1. Name of the medicinal product

Otosporin Ear Drops

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2. Qualitative and quantitative composition

Polymyxin B Sulphate EP 10,000 units per ml

Neomycin Sulphate EP 3,400 units per ml

Hydrocortisone EP 1.0% w/v

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3. Pharmaceutical form

Liquid for topical application to humans

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4. Clinical particulars

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4.1 Therapeutic indications

Otosporin Ear Drops are indicated for the treatment of otitis externa due to, or complicated by, bacterial infection.

Route of Administration


In Vitro Activity

Otosporin Ear Drops are active against a wide range of bacterial pathogens. The range of activity includes:-

Gram-Positive Organisms:

Staphylococcus Epidermis and Staphylococcus Aureus:

Gram-Negative Organisms:

Enterobacter Spp.

Escherichia Spp.

Haemophilus Spp.

Klebsiella Spp.

Proteus Spp.

Pseudomonas Aeruginosa

Otosporin Ear Drops are not expected to be active against streptococci, including Streptococcus Pyogenes

Hydrocortisone possesses anti-inflammatory, anti-allergic and antipruritic activity.

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4.2 Posology and method of administration


Following cleansing and drying of the external auditory meatus and canal as appropriate, three drops should be instilled into the affected ear three or four times daily. Alternatively, a gauze wick may be introduced into the external auditory canal and kept saturated with the solution; the wick may be left in place for 24 to 48 hours.

Treatment should not be continued for more than 7 days without medical supervision.

Soap should not be used for cleansing of the external auditory meatus and canal as it may inactivate the antibiotics.


Otosporin Ear Drops are suitable for use in children ( 3 years and over) at the same dose as adults. A possibility of increased absorption exists in very young children, thus Otosporin Ear Drops are not recommended in neonates and infants (<3 years). (See 4.3 Contra-indications, 4.4 Special Warnings and Precautions for Use).

Use in the Elderly

As for adults. Caution should be exercised in cases where a decrease in renal function exists and significant systemic absorption of neomycin sulphate may occur (see 4.4 Special Warnings and Precautions for Use).

Use in Renal Impairment

Dosage should be reduced in patients with reduced renal function (see 4.4 Special Warnings and Precautions for Use).

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4.3 Contraindications

The use of Otosporin Ear Drops is contra-indicated in patients in whom perforation of the tympanic membrane is known or suspected.

Due to the known ototoxic and nephrotoxic potential of neomycin sulphate, the use of Otosporin Ear Drops in large quantities or on large areas for prolonged periods of time is not recommended in circumstances where significant systemic absorption may occur.

The use of Otosporin Ear Drops is contra-indicated in patients who have demonstrated allergic hypersensitivity to any of the components of the preparation or to cross-sensitising substances such as framycetin, kanamycin, gentamicin and other related antibiotics.

The use of Otosporin Ear Drops is contra-indicated in the presence of untreated viral, fungal and tubercular infections.

A possibility of increased absorption exists in very young children, thus Otosporin Ear Drops are not recommended for use in neonates and infants (up to 3years). In neonates and infants, absorption by immature skin may be enhanced and renal function may be immature.

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4.4 Special warnings and precautions for use

Occasionally, delayed hypersensitivity to corticosteriods may occur. Treatment with topical steroid antibiotic combinations should not be continued for more than seven days in the absence of any clinical improvement, since prolonged use may lead to occult extension of infection due to the masking effect of the steroid. Prolonged use may also lead to skin sensitisation and the emergence of resistant organisms.

Following significant systemic absorption, aminoglycosides such as neomycin can cause irreversible ototoxicity; neomycin and polymyxin B sulphate have nephrotoxic potential and polymyxin B sulphate has neurotoxic potential.

All topically active corticosteroids possess the potential to suppress the pituitary-adrenal axis following systemic absorption. Development of adverse systemic effects due to the hydrocortisone component of Otosporin Ear Drops is considered to be unlikely, although the recommended dosage should not be exceeded, particularly in infants.

Prolonged, unsupervised, use should be avoided as it may lead to irreversible partial or total deafness, especially in the elderly and in patients with impaired renal function. In renal impairment the plasma clearance of neomycin is reduced (see Dosage in Renal Impairment).

Use in the immediate pre- and post- operative period is not advised as neomycin may rarely cause neuro-muscular block; because it potentiates skeletal muscle relaxant drugs, it may cause respiratory depression and arrest.

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4.5 Interaction with other medicinal products and other forms of interaction

Following significant systemic absorption, both neomycin sulphate and polymyxin b sulphate can intensify and prolong the respiratory depressant effects of neuromuscular blocking agents.

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4.6 Pregnancy and lactation

There is little information to demonstrate the possible effect of topically applied neomycin in pregnancy and lactation. However, neomycin present in maternal blood can cross the placenta and may give rise to a theoretical risk of foetal toxicity thus use of Otosporin Ear Drops is not recommended in pregnancy or lactation.

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4.7 Effects on ability to drive and use machines

None known.

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4.8 Undesirable effects

The incidence of allergic hypersensitivity reactions to neomycin sulphate in the general population is low. There is, however, an increased incidence of hypersensitivity to neomycin in certain selected groups of patients in dermatological practice, particularly those with venous stasis eczema and ulceration, and chronic otitis externa.

Allergic hypersensitivity reactions following topical application of polymyxin B sulphate and hydrocortisone are rare.

Allergic hypersensitivity to neomycin following topical use may manifest itself as an eczematous exacerbation with reddening, scaling, swelling and itching or as a failure of the lesion to heal.

Stinging and burning have occasionally been reported when Otosporin Ear Drops gained access to the middle ear.

Otosporin Ear Drops should only be used in the ear and are not suitable for use in the eye.

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4.9 Overdose

Symptoms and signs:-

Possible symptoms or signs associated with excessive use of Otosporin Ear Drops are those due to significant systemic absorption (see Special Warnings and Precautions for Use).


Use of the product should be stopped and the patient's general status, hearing acuity, renal and neuromuscular functions should be monitored.

In overdose, blood concentrations of neomycin sulphate, and polymyxin B sulphate should be determined. Haemodialysis may reduce the serum level of neomycin sulphate.

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5. Pharmacological properties

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5.1 Pharmacodynamic properties

Otosporin solution is a bactericidal preparation active against all the pathogens commonly found in bacterial infections of the ear. Polymyxin B is bactericidal against a wide range of gram negative bacilli including Pseudomonas Spp., Escherichea coli, Enterobacter Spp., Klebsiella Spp., and Haemophilus influenzae. It exerts a bactericidal effect by binding to acid phospholipids in the cell wall and membranes of the bacterium, thereby rendering ineffective the osmotic barrier normally provided by the cell membrane. This leads to escape of the cell contents and the death of the organism.

Neomycin sulphate is bactericidal against a wide range of gram positive and negative bacterial pathogens including staphylococci, streptococci, Escherichia, Enterobacter, Klebsiella, Haemophilus, Proteus, Salmonella and Shigella species. It is also active against some strains of the pseudomonas aeruginosa and against mycobacterium tuberculosis and Neisseria gonorrhoea. Neomycin exerts its bactericidal effect by interfering with the protein synthesis of susceptible organisms.

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5.2 Pharmacokinetic properties

No data are available regarding the pharmacokinetics of this product. However since this is a topical preparation and significant systemic absorption is unlikely to occur, the data are irrelevant.

Systemically absorbed neomycin is predominantly excreted by the kidney and the total amount excreted in the urine varies between 30% and 50%. The pharmacokinetics of systemically absorbed polymyxin B has been described.

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5.3 Preclinical safety data

None stated.

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6. Pharmaceutical particulars

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6.1 List of excipients

Cetostearyl Alcohol EP

Sorbitan Laurate BP

Polysorbate 20 EP

Methyl Hydroxybenzoate EP

Dilute Sulphuric Acid BP

Purified Water EP

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6.2 Incompatibilities

None known

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6.3 Shelf life

36 months

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6.4 Special precautions for storage

Do not store above 25°C

Protect from light

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6.5 Nature and contents of container

Polypropylene bottles with integral nozzles and pilfer proof caps

5ml or 10ml pack sizes

Not all pack sizes may be marketed

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6.6 Special precautions for disposal and other handling

None stated.

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7. Marketing authorisation holder

The Wellcome Foundation Ltd

980 Great West Road


Middlesex TW8 9GS

United Kingdom

Trading as

GlaxoSmithKline UK

Stockley Park West


Middlesex UB11 1BT

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8. Marketing authorisation number(s)


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9. Date of first authorisation/renewal of the authorisation

21 May 2008

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10. Date of revision of the text

06 November 2012

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