| 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 |