Product NDC: | 0498-1070 |
Proprietary Name: | Multi Symptom Cold |
Non Proprietary Name: | Acetaminophen, Dextromethorphan, Phenylephrine, Guaifenesin |
Active Ingredient(s): | 325; 15; 200; 162 mg/1; mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan, Phenylephrine, Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0498-1070 |
Labeler Name: | North Safety Products LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120424 |
Package NDC: | 0498-1070-50 |
Package Description: | 250 CARTON in 1 CARTON (0498-1070-50) > 125 CARTON in 1 CARTON (0498-1070-25) > 50 PACKET in 1 CARTON (0498-1070-10) > 2 TABLET in 1 PACKET (0498-1070-01) |
NDC Code | 0498-1070-50 |
Proprietary Name | Multi Symptom Cold |
Package Description | 250 CARTON in 1 CARTON (0498-1070-50) > 125 CARTON in 1 CARTON (0498-1070-25) > 50 PACKET in 1 CARTON (0498-1070-10) > 2 TABLET in 1 PACKET (0498-1070-01) |
Product NDC | 0498-1070 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromethorphan, Phenylephrine, Guaifenesin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120424 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | North Safety Products LLC |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 325; 15; 200; 162 |
Strength Unit | mg/1; mg/1; mg/1; mg/1 |
Pharmaceutical Classes |