| Product NDC: | 59779-461 |
| Proprietary Name: | Flu Relief BP |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan HBr, Chlorpheniramine maleate |
| Active Ingredient(s): | 500; 2; 15 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan HBr, Chlorpheniramine maleate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59779-461 |
| Labeler Name: | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050601 |
| Package NDC: | 59779-461-09 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (59779-461-09) > 20 TABLET, FILM COATED in 1 BLISTER PACK |
| NDC Code | 59779-461-09 |
| Proprietary Name | Flu Relief BP |
| Package Description | 1 BLISTER PACK in 1 CARTON (59779-461-09) > 20 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 59779-461 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan HBr, Chlorpheniramine maleate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20050601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | WOONSOCKET PRESCRIPTION CENTER,INCORPORATED |
| Substance Name | ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE |
| Strength Number | 500; 2; 15 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |