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GAVISCON DOUBLE ACTION CHEW TAB 32/TAB
GAVISCON DOUBLE ACTION CHEW TAB 32/TAB
21.1
GAVISCON DOUBLE ACTION CHEW TAB 32/TAB

Frequently bought together

Brand : GAVISCON

GAVISCON DOUBLE ACTION CHEW TAB 32/TAB

21.1
  • Sku : I-022926
  • Key features

    Gaviscon Double Action Chewable Tablet 250,187.5,106. is a chewable tablet formulation containing sodium alginate 250 mg, calcium carbonate 187.5 mg and sodium bicarbonate 106.5 mg. Sodium alginate forms a viscous, near‑neutral raft that floats on stomach contents to reduce reflux while calcium carbonate and sodium bicarbonate neutralise gastric acid and support raft formation, raising gastric pH. It provides symptomatic relief of gastro‑oesophageal reflux, including acid regurgitation, heartburn and post‑prandial dyspepsia, and is suitable for pregnancy‑related reflux symptoms. Available OTC as chewable tablets in a 32‑tablet pack.

     

    • Brand: GAVISCON
    • Active Ingredient: SODIUM ALGINATE 250mg, CALCIUM CARBONATE 187.5mg, SODIUM BICARBONATE 106.5mg
    • Strength: 250,187.5,106.5mg
    • Dosage Form: Chewable tablet
    • Pack Size: 32 Tablets
    • Route: Oral use
    • Prescription Status: OTC
    • Therapeutic Class: Gastrointestinal
    • Pharmacological Group: Peptic Ulcer & GERD Drugs
    • Drug Class: Alginate-based antacid; raft-forming anti-reflux agent (A02BX).
    • Manufacturer: RECKITT BENCKISER HEALTHCARE INTERNATIONAL
    • Country of Origin: United Kingdom
    • SFDA Registration No.: 1901268947
    • Shelf Life: 24 months
    • Storage: store below 30°c
    • Gi Condition: Acid Reflux/GERD

Frequently bought together

Description

Indications

Approved Uses

Symptomatic relief of gastro‑oesophageal reflux (acid regurgitation/heartburn) and indigestion/dyspepsia related to reflux, including post‑prandial symptoms; may be used in pregnancy for reflux symptoms.

Dosage & Administration

How to Take

Chew tablets thoroughly before swallowing. Take after meals and at bedtime. Do not swallow whole. Can be taken without water.

Drug Interactions

Food Interaction

Take after meals and at bedtime; post‑prandial dosing improves raft formation and clinical effect.

Special Populations

Liver Impairment

No adjustment needed.

Storage & Patient Advice

Stopping the Medicine

Safe to stop anytime; no tapering required

Pharmacology

Mechanism of Action

Sodium alginate reacts with gastric acid to form a viscous, near‑neutral ‘raft’ that floats on stomach contents and reduces reflux; sodium bicarbonate and calcium carbonate neutralize acid and support raft formation/raise gastric pH.

Onset of Action

Rapid-within minutes (typically ~3-5 minutes).

Duration of Effect

Up to about 4 hours (often ~2-4 hours).

Half-Life

Not applicable / not clinically meaningful (local GI action with minimal systemic absorption).

Bioavailability

Negligible systemic bioavailability; primarily local gastric action (raft formation + antacid effect).

Metabolism

Not systemically metabolized; alginate is not absorbed, and carbonate/bicarbonate are consumed in acid-base neutralization in the stomach.

Excretion

Alginate raft is not absorbed and is eliminated via the GI tract (feces); absorbed sodium/calcium (if any) are handled physiologically and excreted mainly renally.

Protein Binding

Not applicable (no meaningful systemic absorption; protein binding not relevant).

Product Information

Available Dosage Forms

Chewable tablet (this specific SFDA-registered product).

Gi Condition

Acid Reflux/GERD

 

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  • Any discrepancy between the information provided and the product's package insert or SFDA guidelines
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