LABLIN

This brand name is authorized in Nigeria.

Active ingredients

The drug LABLIN contains a combination of these active pharmaceutical ingredients (APIs):

`1`	Diphenhydramine UNII `TC2D6JAD40` - DIPHENHYDRAMINE HYDROCHLORIDE
	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.
	Read more about Diphenhydramine
`2`	Ammonium chloride UNII `01Q9PC255D` - AMMONIUM CHLORIDE
	Read more about Ammonium chloride
`3`	Sodium citrate UNII `1Q73Q2JULR` - SODIUM CITRATE, UNSPECIFIED FORM
	Sodium citrate has no relevant pharmacodynamic activity other than that caused by its alkalinity (e.g. its gastric acid neutralising capacity). Sodium citrate is a non-particulate antacid for use by mouth to prior to general anaesthesia for caesarean section.
	Read more about Sodium citrate
`4`	Menthol UNII `L7T10EIP3A` - MENTHOL, UNSPECIFIED FORM
	Read more about Menthol

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group		Classification
R06AA52	Diphenhydramine, combinations	R Respiratory system → R06 Antihistamines for systemic use → R06A Antihistamines for systemic use → R06AA Aminoalkyl ethers
Discover more medicines within R06AA52

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country	Identification scheme	Identifier(s)
NG	Registered Drug Product Database	04-3109
Switch country to Nigeria in order to find specific presentations of LABLIN

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