This information is intended for use by health professionals

1. Name of the medicinal product


2. Qualitative and quantitative composition

Contains not less than 8.820g Ammonia Liquor 880/890 and 0.539g Eucalyptus Oil.

For a full list of excipients, see section 6.1.

3. Pharmaceutical form

White granules.

4. Clinical particulars
4.1 Therapeutic indications

1) Traditionally used for the symptomatic relief of catarrh and head colds.

4.2 Posology and method of administration


Inhale vapour through nostrils as required.

Do not use for children under 3 months of age.

Method of Administration


4.3 Contraindications

Do not use for children under 3 months of age.

4.4 Special warnings and precautions for use

None known.

The product labelling includes the following statements:

Not to be taken.

If symptoms persist consult your doctor.

Keep out of the reach and sight of children.

4.5 Interaction with other medicinal products and other forms of interaction

None known.

4.6 Pregnancy and lactation

No special precautions are considered necessary.

4.7 Effects on ability to drive and use machines

None known.

4.8 Undesirable effects

None known.

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; website: or search for MHRA Yellow Card in the Google Play or Apple App Store.

4.9 Overdose

No special requirements are anticipated.

5. Pharmacological properties
5.1 Pharmacodynamic properties

ATC code:R01A X

Ammonia is employed in the product as a reflex stimulant.

Eucalyptus oil is an essential oil.

5.2 Pharmacokinetic properties

Not applicable.

5.3 Preclinical safety data

There are no pre-clinical data of relevance to the prescriber which are additional to that already included in other sections of the SPC.

6. Pharmaceutical particulars
6.1 List of excipients

Also contains glycerol, soft soap, tapioca, water.

6.2 Incompatibilities

None known.

6.3 Shelf life


Three years from the date of manufacture.

Shelf-life after dilution/reconstitution

Not applicable.

Shelf-life after first opening

Not applicable.

6.4 Special precautions for storage

Store in a cool place.

6.5 Nature and contents of container

The product container is a uniquely-shaped amber glass bottle with black HDPE cap with LDPE liner.

Pack size: 17ml

6.6 Special precautions for disposal and other handling

Not applicable.

Administrative Data

7. Marketing authorisation holder

Teva UK Limited

Ridings Point,

Whistler Drive,


WF10 5HX,

United Kingdom

8. Marketing authorisation number(s)

PL 00289/2207

9. Date of first authorisation/renewal of the authorisation

16.10.86 (Product Licence of Right issued: 27.7.73)

Renewed: 14.5.92; 11.7.97

10. Date of revision of the text