Gelusil
Active substance: ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE, UNSPECIFIED, SILICON DIOXIDE
TABLET, CHEWABLE · ALUMINUM HYDROXIDE 200 mg/1, MAGNESIUM HYDROXIDE 200 mg/1, DIMETHICONE, UNSPECIFIED 24 mg/1, SILICON DIOXIDE 1 mg/1
United StatesActive
Marketing holder: WellSpring Pharmaceutical Corporation
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- ALUMINUM HYDROXIDE · 200 mg/1
- MAGNESIUM HYDROXIDE · 200 mg/1
- DIMETHICONE, UNSPECIFIED · 24 mg/1
- SILICON DIOXIDE · 1 mg/1
Registration
- Registration number
- 65197-300
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 65197-300 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 65197-300 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 65197-300 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 65197-300 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 65197-300 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 65197-300 · Verified 2026-10-09 · open in source