Generated automatically from the NAFDAC register, WHO alerts and community data as of today. Not medical advice — always follow your doctor or pharmacist.
From the official U.S. FDA label for Nugel Suspension, the active ingredient registered with NAFDAC.
• for hand sanitizing to decrease bacteria on skin when water and soap are not avaliable • recommended for repeated use
Antimicrobial
For external use only. Flammable keep away from fire or flame. When using this product do not use in or near eyes, if contact occurs, flush thoroughly with water. Stop use and contact a doctor if irritation or redness persists for more than 72 hours.
Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.
Nugel Suspension contains Aluminium hydroxide; Magnesium hydroxide; Magnesium trisilicate; Alginic acid; Simeticone (85 mg/5 mL; 85 mg/5 mL; 85 mg/5 mL; 70 mg/5 mL; 50 mg/5 mL), as suspension, according to its NAFDAC registration record.
Yes. Nugel Suspension is listed on the NAFDAC register under registration number B4-3199, and its registration is active as of 5 November 2026.
No WHO falsified or substandard medical product alert currently matches Nugel Suspension in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number B4-3199, 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.
• for hand sanitizing to decrease bacteria on skin when water and soap are not avaliable • recommended for repeated use (Summarised from the official U.S. FDA label for Nugel Suspension. Always follow your doctor or pharmacist.)
Reviews are personal experiences from RxVerify users, not medical advice. Report side effects to your doctor and to NAFDAC.