| Product NDC: | 37808-668 |
| Proprietary Name: | night time |
| Non Proprietary Name: | Dextromethorphan HBr, Doxylamine succinate |
| Active Ingredient(s): | 30; 12.5 mg/30mL; mg/30mL & nbsp; Dextromethorphan HBr, Doxylamine succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 37808-668 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030225 |
| Package NDC: | 37808-668-40 |
| Package Description: | 355 mL in 1 BOTTLE (37808-668-40) |
| NDC Code | 37808-668-40 |
| Proprietary Name | night time |
| Package Description | 355 mL in 1 BOTTLE (37808-668-40) |
| Product NDC | 37808-668 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan HBr, Doxylamine succinate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20030225 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | H E B |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 30; 12.5 |
| Strength Unit | mg/30mL; mg/30mL |
| Pharmaceutical Classes |