| NDC Code | 62372-504-12 |
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| Package Description | 355 mL in 1 BOTTLE, PLASTIC (62372-504-12) |
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| Product NDC | 62372-504 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Mylanta Maximum Strength Vanilla Caramel Flavor |
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| Non-Proprietary Name | Antacid And Anti Gas Aluminum Hydroxide Magnesium Hydroxide And Simethicone |
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| Dosage Form | SUSPENSION |
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| Usage | ORAL |
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| Start Marketing Date | 20160321 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M001 |
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| Manufacturer | Infirst Healthcare Inc. |
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| Substance Name | ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE |
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| Strength | 800; 80; 800 |
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| Strength Unit | mg/10mL; mg/10mL; mg/10mL |
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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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