Product NDC: | 59779-220 |
Proprietary Name: | CVS Pharmacy Daytime Severe Cough and Cold |
Non Proprietary Name: | Acetaminophen, Dextromethorphan HBr and Phenylephrine HCL |
Active Ingredient(s): | 650; 20; 10 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan HBr and Phenylephrine HCL |
Administration Route(s): | ORAL |
Dosage Form(s): | GRANULE, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-220 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130401 |
Package NDC: | 59779-220-06 |
Package Description: | 6 GRANULE, FOR SOLUTION in 1 BOX (59779-220-06) |
NDC Code | 59779-220-06 |
Proprietary Name | CVS Pharmacy Daytime Severe Cough and Cold |
Package Description | 6 GRANULE, FOR SOLUTION in 1 BOX (59779-220-06) |
Product NDC | 59779-220 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Dextromethorphan HBr and Phenylephrine HCL |
Dosage Form Name | GRANULE, FOR SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20130401 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CVS Pharmacy |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 650; 20; 10 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |