| NDC Code | 65197-300-10 |
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| Package Description | 10 BLISTER PACK in 1 CARTON (65197-300-10) / 10 TABLET, CHEWABLE in 1 BLISTER PACK |
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| Product NDC | 65197-300 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Gelusil |
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| Non-Proprietary Name | Alumina, Magnesia, Simethicone |
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| Dosage Form | TABLET, CHEWABLE |
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| Usage | ORAL |
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| Start Marketing Date | 20080924 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M001 |
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| Manufacturer | WellSpring Pharmaceutical Corporation |
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| Substance Name | ALUMINUM HYDROXIDE; DIMETHICONE, UNSPECIFIED; MAGNESIUM HYDROXIDE; SILICON DIOXIDE |
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| Strength | 200; 24; 200; 1 |
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| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Skin Barrier Activity [PE], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
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