Product NDC: | 0363-0503 |
Proprietary Name: | Daytime Multi-Symptom Severe Cold |
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: | 0363-0503 |
Labeler Name: | WALGREEN CO. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20050804 |
Package NDC: | 0363-0503-08 |
Package Description: | 2 BLISTER PACK in 1 CARTON (0363-0503-08) > 12 TABLET, COATED in 1 BLISTER PACK |
NDC Code | 0363-0503-08 |
Proprietary Name | Daytime Multi-Symptom Severe Cold |
Package Description | 2 BLISTER PACK in 1 CARTON (0363-0503-08) > 12 TABLET, COATED in 1 BLISTER PACK |
Product NDC | 0363-0503 |
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 | WALGREEN CO. |
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 |