View drug registration information details.
Items | Registration information |
ID | 512 |
No | 512 |
Brand Name | GAVISCON DUAL ACTION LIQUID |
Ingredients | SODIUM ALGINATE 500 MG, SODIUM BICARBONATE 213 MG, CALCIUM CARBONATE 325 MG |
Dosage Form | SUSPENSION |
Primary Packaging | SACHET, BOTTLE |
Storage | DO NOT STORE ABOVE 30C |
Shelf Life | 2 YEARS |
Pack Size | BOX OF 24 SACHETS X 10ML, BOX OF 150 ML/BOTTLE |
Dispensing Category | Prescription only |
ATC Classification | A02BX |
Pharmaceutical Class | ANTACIDS, ANTIULCERANTS |
Indications | TREATMENT OF SYMPTOMS RESULTING FROM THE REFLUX OF ACID, BILE AND PEPSIN INTO THE OESOPHAGUS SUCH AS ACID REGURGITATION, HEARTBURN AND INDIGESTION, FOR EXAMPLE FLLOWING MEALS OR DURING PREGNANCY, AND FOR SYMOMS OF EXCESS STOMACH ACID, CAN ALSO BE USED TO TREAT THE SYMPTOMS OF GASTRO-ESOPHAGEAL REFLUX DURING CONCOMITANT TREATMENT WITH OR FOLLOWING WITHDRAWAL OF ACID SUPPRESSION THERAPY |
Contraindications | HYPERSENSITIVITY TO ACTIVE INGREDIENT, MODERATE OR SEVERE RENAL INSUFFICIENCY |
Side Effects | ANAPHYLACTIC REACTION, ANAPHYLACTOID REACTION, URTICARIA, BROMCHOSPASM |
Unit Price | |
EDL |
No |
Description | OPAQUE OFF-WHITE TO CREAM VISCOUS SUSPENSION |
Note | |
License Owner | DKSH LAOS COMPANY LIMITED |
Manufacturer | RECKITT BENCKISER HEALTHCARE(UK)LIMITED |
Country | UNITED KINGDOM |
Import Registration No | PL00063/0552 |
Import Registration Date | 2008-06-25 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2021-04-02 |
FDD Registration No | 01 I 5372/23 |
FDD Registration Date | 2023-01-23 |
Expiry Date | 2026-01-22 |
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