| Product NDC: | 0363-0335 |
| Proprietary Name: | nighttime cold and flu relief |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan HBr, Doxylamine succinate |
| Active Ingredient(s): | 650; 30; 12.5 mg/30mL; mg/30mL; mg/30mL & nbsp; Acetaminophen, Dextromethorphan HBr, Doxylamine succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0363-0335 |
| Labeler Name: | Walgreen Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110808 |
| Package NDC: | 0363-0335-30 |
| Package Description: | 177 mL in 1 BOTTLE (0363-0335-30) |
| NDC Code | 0363-0335-30 |
| Proprietary Name | nighttime cold and flu relief |
| Package Description | 177 mL in 1 BOTTLE (0363-0335-30) |
| Product NDC | 0363-0335 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan HBr, Doxylamine succinate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110808 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Walgreen Company |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 650; 30; 12.5 |
| Strength Unit | mg/30mL; mg/30mL; mg/30mL |
| Pharmaceutical Classes |