INSTILLAGEL

This brand name is authorized in Austria, Canada, Cyprus, France, Hong Kong SAR China, Ireland, Israel, Netherlands, New Zealand, UK.

Active ingredients

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

1
UNII V13007Z41A - LIDOCAINE HYDROCHLORIDE
 

Lidocaine, like other local anaesthetics, causes a reversible blockade of impulse propagation along nerve fibres by preventing the inward movement of sodium ions through the nerve membrane. Local anaesthetics of the amide-type are thought to act within the sodium channels of the nerve membrane.

 
Read more about Lidocaine
2
UNII MOR84MUD8E - CHLORHEXIDINE GLUCONATE
 

Chlorhexidine is an antimicrobial agent, active against a broad spectrum of Gram-positive and Gram-negative organisms, yeasts, fungi, opportunistic anaerobes and aerobes. Chlorhexidine is mainly a "membrane-acting" agent that destroys the outer membrane of the bacteria. It is inactive on bacterial spores unless the temperatures are high.

 
Read more about Chlorhexidine

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 INSTILLAGEL Gel MPI, EU: SmPC Υπουργείο Υγείας (CY)

Medicine classification

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

ATC Group Classification
N01BB52 Lidocaine, combinations N Nervous system → N01 Anesthetics → N01B Anesthetics, local → N01BB Amides
Discover more medicines within N01BB52

Authorization and marketing

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

Country Identification scheme Identifier(s)
CA Health Products and Food Branch 02294990
FR Base de données publique des médicaments 62686809
GB Medicines & Healthcare Products Regulatory Agency 85538, 85540
HK Department of Health Drug Office 17013
IE Health Products Regulatory Authority 30589, 83720
IL מִשְׂרַד הַבְּרִיאוּת 8687
NL Z-Index G-Standaard 13896555, 13897039
NL Z-Index G-Standaard, PRK 81957, 81965
NZ Medicines and Medical Devices Safety Authority 14909

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