DULCOLAX

This brand name is authorized in Austria, Australia, Brazil, Canada, Cyprus, France, Hong Kong, Croatia, Ireland, Malta, Mexico, Netherlands, New Zealand, Romania, Singapore, United Kingdom, United States, South Africa

Active ingredients

The drug DULCOLAX contains one active pharmaceutical ingredient (API):

1 Bisacodyl
UNII 10X0709Y6I - BISACODYL

Bisacodyl is a locally acting laxative from the diphenylmethane derivatives group having a dual action. As a contact laxative, for which also antiresorptive hydragogue effects have been described, bisacodyl stimulates after hydrolysis in the large intestine, the mucosa of both the large intestine and of the rectum. Stimulation of the mucosa of the large intestine results in colonic peristalsis with promotion of accumulation of water, and consequently electrolytes, in the colonic lumen. This results in a stimulation of defecation, reduction of transit time and softening of the stool. Stimulation of the rectum causes increased motility and a feeling of rectal fullness. The rectal effect may help to restore the “call to stool” although its clinical relevance remains to be established.

Read about Bisacodyl

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
DULCOLAX Gastro-resistant tablets Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
A06AB02 Bisacodyl A Alimentary tract and metabolism → A06 Laxatives → A06A Laxatives → A06AB Contact laxatives
Discover more medicines within A06AB02

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 10578R, 1260H, 3250C
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 576720050064617
Country: CA Health Products and Food Branch Identifier(s): 00003875, 00254142, 02397854
Country: FR Base de données publique des médicaments Identifier(s): 64835956, 65323898
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 107527, 135340, 135347, 19164, 30744, 30745
Country: HK Department of Health Drug Office Identifier(s): 02708
Country: MT Medicines Authority Identifier(s): MA1470/00401, MA1470/00402, MA1470/00501
Country: MX Comisión Federal para la Protección contra Riesgos Sanitarios Identifier(s): 47191
Country: NL Z-Index G-Standaard, PRK Identifier(s): 4960, 884
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 18027, 461, 463
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W68445001, W68446001
Country: SG Health Sciences Authority Identifier(s): 02663P, 02668P, 02669P
Country: US FDA, National Drug Code Identifier(s): 41167-0101, 41167-0200, 41167-0210, 41167-0290, 41167-0400
Country: ZA Health Products Regulatory Authority Identifier(s): E/11.5/531, E/11.5/532, E/11.5/534

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