Product NDC: | 59779-666 |
Proprietary Name: | Night Time Cough and Sore Throat Cool Blast |
Non Proprietary Name: | Tylenol Cough and Sore Throat |
Active Ingredient(s): | 1000; 30; 12.5 mg/30mL; mg/30mL; mg/30mL & nbsp; Tylenol Cough and Sore Throat |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-666 |
Labeler Name: | CVS |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090708 |
Package NDC: | 59779-666-34 |
Package Description: | 237 mL in 1 BOTTLE, PLASTIC (59779-666-34) |
NDC Code | 59779-666-34 |
Proprietary Name | Night Time Cough and Sore Throat Cool Blast |
Package Description | 237 mL in 1 BOTTLE, PLASTIC (59779-666-34) |
Product NDC | 59779-666 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Tylenol Cough and Sore Throat |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 20090708 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CVS |
Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
Strength Number | 1000; 30; 12.5 |
Strength Unit | mg/30mL; mg/30mL; mg/30mL |
Pharmaceutical Classes |