| Product NDC: | 59779-656 | 
| Proprietary Name: | Daytime | 
| Non Proprietary Name: | acetaminophen, dextromethorphan hbr, phenylephrine hcl | 
| Active Ingredient(s): | 325; 10; 5 mg/15mL; mg/15mL; mg/15mL & nbsp; acetaminophen, dextromethorphan hbr, phenylephrine hcl | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59779-656 | 
| Labeler Name: | CVS Pharmacy | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part341 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20060609 | 
| Package NDC: | 59779-656-38 | 
| Package Description: | 295 mL in 1 BOTTLE (59779-656-38) | 
| NDC Code | 59779-656-38 | 
| Proprietary Name | Daytime | 
| Package Description | 295 mL in 1 BOTTLE (59779-656-38) | 
| Product NDC | 59779-656 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | acetaminophen, dextromethorphan hbr, phenylephrine hcl | 
| Dosage Form Name | LIQUID | 
| Route Name | ORAL | 
| Start Marketing Date | 20060609 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | CVS Pharmacy | 
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE | 
| Strength Number | 325; 10; 5 | 
| Strength Unit | mg/15mL; mg/15mL; mg/15mL | 
| Pharmaceutical Classes |