| Product NDC: | 11822-0880 |
| Proprietary Name: | antacid |
| Non Proprietary Name: | Aluminum hydroxide, Magnesium carbonate |
| Active Ingredient(s): | 160; 105 mg/1; mg/1 & nbsp; Aluminum hydroxide, Magnesium carbonate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11822-0880 |
| Labeler Name: | Rite Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part331 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19970807 |
| Package NDC: | 11822-0880-7 |
| Package Description: | 100 TABLET, CHEWABLE in 1 BOTTLE (11822-0880-7) |
| NDC Code | 11822-0880-7 |
| Proprietary Name | antacid |
| Package Description | 100 TABLET, CHEWABLE in 1 BOTTLE (11822-0880-7) |
| Product NDC | 11822-0880 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum hydroxide, Magnesium carbonate |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 19970807 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rite Aid Corporation |
| Substance Name | ALUMINUM HYDROXIDE; MAGNESIUM CARBONATE |
| Strength Number | 160; 105 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |