| Product NDC: | 11673-645 |
| Proprietary Name: | PE multi-stymptom cold and cough relief |
| Non Proprietary Name: | Acetaminophen, Dextromathorphan HBr, Gauifenesin, Phenylephrine HCl |
| Active Ingredient(s): | 325; 10; 100; 5 mg/1; mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromathorphan HBr, Gauifenesin, Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11673-645 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20070222 |
| Package NDC: | 11673-645-09 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (11673-645-09) > 20 CAPSULE, COATED in 1 BLISTER PACK |
| NDC Code | 11673-645-09 |
| Proprietary Name | PE multi-stymptom cold and cough relief |
| Package Description | 1 BLISTER PACK in 1 CARTON (11673-645-09) > 20 CAPSULE, COATED in 1 BLISTER PACK |
| Product NDC | 11673-645 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromathorphan HBr, Gauifenesin, Phenylephrine HCl |
| Dosage Form Name | CAPSULE, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20070222 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Target Corporation |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 100; 5 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |