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Rx Act Antacid
Rx Act Antacid - 37808-357-40 - (Aluminum hydroxide, Magnesium hydroxide, Simethicone)
Drug Information of Rx Act Antacid
| Product NDC: | 37808-357 |
| Proprietary Name: | Rx Act Antacid |
| Non Proprietary Name: | Aluminum hydroxide, Magnesium hydroxide, Simethicone |
| Active Ingredient(s): | 200; 20; 200 mg/5mL; mg/5mL; mg/5mL & nbsp; Aluminum hydroxide, Magnesium hydroxide, Simethicone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rx Act Antacid
| Product NDC: | 37808-357 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part332 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19920618 |
Package Information of Rx Act Antacid
| Package NDC: | 37808-357-40 |
| Package Description: | 355 mL in 1 BOTTLE (37808-357-40) |
NDC Information of Rx Act Antacid
| NDC Code | 37808-357-40 |
| Proprietary Name | Rx Act Antacid |
| Package Description | 355 mL in 1 BOTTLE (37808-357-40) |
| Product NDC | 37808-357 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Aluminum hydroxide, Magnesium hydroxide, Simethicone |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19920618 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | H E B |
| Substance Name | ALUMINUM HYDROXIDE; DIMETHICONE; MAGNESIUM HYDROXIDE |
| Strength Number | 200; 20; 200 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
