| Product NDC: | 11822-0503 |
| Proprietary Name: | Head Congestion Cold DayTime |
| Non Proprietary Name: | Acetaminophen, Phenylephrine HCl, Dextromethorphan HBr and Guiafenesin |
| Active Ingredient(s): | 325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Phenylephrine HCl, Dextromethorphan HBr and Guiafenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11822-0503 |
| Labeler Name: | Rite Aid |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050804 |
| Package NDC: | 11822-0503-8 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (11822-0503-8) > 24 TABLET, COATED in 1 BLISTER PACK |
| NDC Code | 11822-0503-8 |
| Proprietary Name | Head Congestion Cold DayTime |
| Package Description | 1 BLISTER PACK in 1 CARTON (11822-0503-8) > 24 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 11822-0503 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Phenylephrine HCl, Dextromethorphan HBr and Guiafenesin |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20050804 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Rite Aid |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 200; 5 |
| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |