Product NDC: | 59779-041 |
Proprietary Name: | CVS Nighttime Cold/Flu Relief |
Non Proprietary Name: | acetaminophen, dextromethorphan hydrobromide and doxylamine succinate |
Active Ingredient(s): | 500; 15; 6.25 mg/15mL; mg/15mL; mg/15mL & nbsp; acetaminophen, dextromethorphan hydrobromide and doxylamine succinate |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-041 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090709 |
Package NDC: | 59779-041-40 |
Package Description: | 355 mL in 1 BOTTLE (59779-041-40) |
NDC Code | 59779-041-40 |
Proprietary Name | CVS Nighttime Cold/Flu Relief |
Package Description | 355 mL in 1 BOTTLE (59779-041-40) |
Product NDC | 59779-041 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | acetaminophen, dextromethorphan hydrobromide and doxylamine succinate |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20090709 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CVS Pharmacy |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 500; 15; 6.25 |
Strength Unit | mg/15mL; mg/15mL; mg/15mL |
Pharmaceutical Classes |