| Product NDC: | 59779-221 | 
| Proprietary Name: | CVS Pharmacy Nighttime Severe Cough and Cold | 
| Non Proprietary Name: | Acetaminophen, Diphenhydramine HCL and Phenylephrine HCL | 
| Active Ingredient(s): | 650; 25; 10 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Diphenhydramine HCL and Phenylephrine HCL | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | GRANULE, FOR SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59779-221 | 
| Labeler Name: | CVS Pharmacy | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20130325 | 
| Package NDC: | 59779-221-06 | 
| Package Description: | 6 GRANULE, FOR SOLUTION in 1 BOX (59779-221-06) | 
| NDC Code | 59779-221-06 | 
| Proprietary Name | CVS Pharmacy Nighttime Severe Cough and Cold | 
| Package Description | 6 GRANULE, FOR SOLUTION in 1 BOX (59779-221-06) | 
| Product NDC | 59779-221 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Acetaminophen, Diphenhydramine HCL and Phenylephrine HCL | 
| Dosage Form Name | GRANULE, FOR SOLUTION | 
| Route Name | ORAL | 
| Start Marketing Date | 20130325 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | CVS Pharmacy | 
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE | 
| Strength Number | 650; 25; 10 | 
| Strength Unit | mg/1; mg/1; mg/1 | 
| Pharmaceutical Classes |