Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.
From the official U.S. FDA label for sodium alginate, the active ingredient registered with NAFDAC.
INDICATIONS: Aids in temporary relief of symptoms from exposure to household radiation such as headaches, difficulty sleeping, fatigue, muscle weakness and itchy skin.† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Aids in temporary relief of symptoms from exposure to household radiation such as headaches, difficulty sleeping, fatigue, muscle weakness and itchy skin.† †Claims based on traditional homeopathic pra …
Professional Use Only If pregnant or breast-feeding, ask a health professional before use. In case of overdose, get medical help or contact a Poison Control Center right away. If condition worsens, seek medical attention. KEEP OUT OF REACH OF CHILDREN Do not use if tamper evident seal is broken or missing. Store in a cool place after opening
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Gaviscon Double Action Liquid contains Sodium alginate; Sodium bicarbonate; Calcium carbonate (250 mg/5 mL; 133.5 mg/5 mL; 80 mg/5 mL), as suspension, according to its NAFDAC registration record.
Yes. Gaviscon Double Action Liquid is listed on the NAFDAC register under registration number A4-9366, and its registration is active as of 27 October 2026.
No WHO falsified or substandard medical product alert currently matches Gaviscon Double Action Liquid in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number A4-9366, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.
INDICATIONS: Aids in temporary relief of symptoms from exposure to household radiation such as headaches, difficulty sleeping, fatigue, muscle weakness and itchy skin.† †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. (Summarised from the official U.S. FDA label for sodium alginate. Always follow your doctor or pharmacist.)
Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.