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McNeil Products Ltd

Foundation Park, Roxborough Way, Maidenhead, Berks, SL6 3UG
Medical Information Direct Line: 01344 864042
Medical Information e-mail: medinfo@its.jnj.com

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Summary of Product Characteristics last updated on the eMC: 13/05/2011
SPC Sudafed Blocked Nose Spray


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1. NAME OF THE MEDICINAL PRODUCT

Non-Drowsy Sudafed Decongestant Nasal Spray

Sudafed Blocked Nose Spray

Sudafed Mucus Relief 0.1% Nasal Spray


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2. QUALITATIVE AND QUANTITATIVE COMPOSITION

This product is an aqueous solution of Xylometazoline Hydrochloride 0.1% w/v presented in a metered-dose pack, delivering 0.14 ml per actuation.

For excipients see 6.1.


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3. PHARMACEUTICAL FORM

Aqueous solution


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4. CLINICAL PARTICULARS

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4.1 Therapeutic indications

This product is indicated for the symptomatic relief of nasal congestion associated with the common cold, influenza, sinusitis, allergic and non-allergic rhinitis, and other upper respiratory tract allergies.


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4.2 Posology and method of administration

Adults and children 12 years and over:

Nasal. One spray to be expressed into each nostril 2-3 times daily, as necessary.

Maximum daily dose: 3 sprays.

Use for more than seven consecutive days is not recommended, [See Undesirable effects].

Children under 12 years:

This product is not recommended for children under 12 years of age.

The Elderly

Experience has indicated that normal adult dosage is appropriate, [See Pharmacokinetics in the elderly].

Hepatic/renal dysfunction

Normal adult dosage is appropriate, [See Pharmacokinetic properties].


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4.3 Contraindications

This product is contraindicated in individuals with known hypersensitivity to the product or any of its constituents.

This product is contraindicated in individuals who are taking or have taken, monoamine oxidase inhibitors within the preceding two weeks.

This product is contraindicated in individuals with hypophysectomy or surgery exposing dura mater.


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4.4 Special warnings and precautions for use

There is minimal systemic absorption with topically applied imidazoline sympathomimetics such as xylometazoline, however, this product should be used with caution in patients suffering coronary artery disease, hypertension, hyperthyroidism or diabetes mellitus.


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4.5 Interaction with other medicinal products and other forms of interaction

Due to the low systemic absorption of xylometazoline when administered intra-nasally, interaction with drugs administered via other routes is considered unlikely.


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4.6 Pregnancy and lactation

No foetal toxicity or fertility studies have been carried out in animals. In view of its potential vasoconstrictor effect, it is advisable to take the precaution of not using this product during pregnancy.


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4.7 Effects on ability to drive and use machines

No special comment - unlikely to produce an effect.


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4.8 Undesirable effects

Xylometazoline nasal preparations are generally well tolerated following short-term use and local side effects are mild and infrequent. Localised burning, stinging, itching, soreness, dryness or irritation and sneezing may occur occasionally. Rarely, nausea and headache may occur.

Rebound congestion has been reported occasionally, particularly following longer-term use of xylometazoline.


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4.9 Overdose

Symptoms and signs

Systemic action is unlikely when applied nasally due to the local vasoconstriction that inhibits absorption. If systemic absorption does occur xylometazoline as an α2-adrenergic agonist could be expected to produce effects similar to those of clonidine with a short lived rise in blood pressure, followed by more prolonged hypotension and sedation.

Treatment

Treatment of overdose should be supportive.


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5. PHARMACOLOGICAL PROPERTIES

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5.1 Pharmacodynamic properties

Xylometazoline is a sympathomimetic amine of the imidazoline class.

It act directly on α-adrenoreceptors but does not act on ßNON-BREAKING HYPHEN (8209)receptors. When used topically as a nasal decongestant, xylometazoline acts rapidly and provides long-lasting relief. Onset of action is within minutes, the decongestant effect being prolonged and lasting for up to 10 hours.


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5.2 Pharmacokinetic properties

Absorption, Distribution, Metabolism and Elimination

Little information is available concerning the absorption, distribution, metabolism and elimination of xylometazoline in man. Absorption into the nasal mucosal tissues is rapid.

Pharmacokinetics in Renal/Hepatic Impairment

There have been no specific studies of this product or xylometazoline in hepatic or renal impairment.

Pharmacokinetics in the Elderly

There have been no specific clinical studies of this product or xylometazoline in the elderly.


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5.3 Preclinical safety data

Mutagenicity

There is insufficient information available to determine whether xylometazoline has mutagenic potential.

Carcinogenicity

There is insufficient information available to determine whether xylometazoline has carcinogenic potential.

Teratogenicity

There is insufficient information available to determine whether xylometazoline has teratogenic potential.

Fertility

No studies have been conducted in animals to determine whether xylometazoline has the potential to impair fertility. There is no information on the effects of this product on fertility.


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6. PHARMACEUTICAL PARTICULARS

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6.1 List of excipients

Benzalkonium chloride solution

Disodium edetate

Sodium dihydrogen phosphate dihydrate

Sodium monohydrogen phosphate dihydrate

Sodium chloride

Sorbitol solution, 70% (Non crystalline)

Purified water


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6.2 Incompatibilities

None known


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6.3 Shelf life

3 years.


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6.4 Special precautions for storage

Do not store above 25°C.


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6.5 Nature and contents of container

Amber glass bottle of either 10 ml or 15 ml nominal fill volume.

The bottle is sealed with an integral snap-on metered 0.14 ml pump consisting of a white plastic actuator and natural polyethylene pull-off overcap.


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6.6 Special precautions for disposal and other handling

None applicable.


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7. MARKETING AUTHORISATION HOLDER

McNeil Products Limited

Foundation Park

Roxborough Way

Maidenhead

Berkshire SL6 3UG

United Kingdom.


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8. MARKETING AUTHORISATION NUMBER(S)

PL 15513/0074


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9. DATE OF FIRST AUTHORISATION/RENEWAL OF THE AUTHORISATION

21/04/99


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10. DATE OF REVISION OF THE TEXT

5 May 2011



More information about this product

Link to this document from your website: http://www.medicines.org.uk/emc/medicine/10498/SPC/


Active Ingredients/Generics

 
   xylometazoline hydrochloride