This brand name is authorized in Cyprus, Ireland, Malta, United Kingdom
The drug BENYLIN contains a combination of these active pharmaceutical ingredients (APIs):
1
Diphenhydramine
UNII TC2D6JAD40 - DIPHENHYDRAMINE HYDROCHLORIDE
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Diphenhydramine is an ethanolamine-derivative antihistamine. It is an antihistamine with anticholinergic and marked sedative effects. It acts by inhibiting the effects on H1-receptors. Diphenhydramine is effective in reducing sleep onset (i.e., time to fall asleep) and increasing the depth and quality of sleep. |
2
Menthol
UNII BZ1R15MTK7 - LEVOMENTHOL
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Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
BENYLIN DRY COUGHS Syrup | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC | |
BENYLIN MUCUS COUGH MAX Oral solution | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
R06AA02 | Diphenhydramine | R Respiratory system → R06 Antihistamines for systemic use → R06A Antihistamines for systemic use → R06AA Aminoalkyl ethers |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 129538, 49465 |
Country: MT | Medicines Authority | Identifier(s): MA1315/00202 |
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