| Product NDC: | 67510-0544 |
| Proprietary Name: | Day Time Cold/Flu Relief |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan, Phenylephrine |
| Active Ingredient(s): | 325; 10; 5 mg/15mL; mg/15mL; mg/15mL & nbsp; Acetaminophen, Dextromethorphan, Phenylephrine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67510-0544 |
| Labeler Name: | Kareway Product, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110906 |
| Package NDC: | 67510-0544-0 |
| Package Description: | 295 mL in 1 BOTTLE (67510-0544-0) |
| NDC Code | 67510-0544-0 |
| Proprietary Name | Day Time Cold/Flu Relief |
| Package Description | 295 mL in 1 BOTTLE (67510-0544-0) |
| Product NDC | 67510-0544 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan, Phenylephrine |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110906 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kareway Product, Inc. |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 5 |
| Strength Unit | mg/15mL; mg/15mL; mg/15mL |
| Pharmaceutical Classes |