| Product NDC: | 0536-3504 |
| Proprietary Name: | Almacone |
| Non Proprietary Name: | Aluminum hydroxide, Magnesium hydroxide, Simethicone |
| Active Ingredient(s): | 200; 20; 200 mg/1; mg/1; mg/1 & nbsp; Aluminum hydroxide, Magnesium hydroxide, Simethicone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0536-3504 |
| Labeler Name: | Rugby Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part332 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100823 |
| Package NDC: | 0536-3504-01 |
| Package Description: | 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0536-3504-01) |
| NDC Code | 0536-3504-01 |
| Proprietary Name | Almacone |
| Package Description | 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0536-3504-01) |
| Product NDC | 0536-3504 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum hydroxide, Magnesium hydroxide, Simethicone |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20100823 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rugby Laboratories, Inc. |
| Substance Name | ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE |
| Strength Number | 200; 20; 200 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |