| Product NDC: | 41250-031 |
| Proprietary Name: | day time nitetime cough |
| Non Proprietary Name: | dextromethorphan hbr, doxylamine succinate |
| Active Ingredient(s): | & nbsp; dextromethorphan hbr, doxylamine succinate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 41250-031 |
| Labeler Name: | Meijer Distribution Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19920110 |
| Package NDC: | 41250-031-01 |
| Package Description: | 1 KIT in 1 CARTON (41250-031-01) * 296 mL in 1 BOTTLE (41250-668-38) * 296 mL in 1 BOTTLE (41250-473-38) |
| NDC Code | 41250-031-01 |
| Proprietary Name | day time nitetime cough |
| Package Description | 1 KIT in 1 CARTON (41250-031-01) * 296 mL in 1 BOTTLE (41250-668-38) * 296 mL in 1 BOTTLE (41250-473-38) |
| Product NDC | 41250-031 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dextromethorphan hbr, doxylamine succinate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19920110 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Meijer Distribution Inc |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |