| Product NDC: | 35418-119 |
| Proprietary Name: | Cough Syrup DM |
| Non Proprietary Name: | Guaifenesin, Dextromethorpham HBr |
| Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; Guaifenesin, Dextromethorpham HBr |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 35418-119 |
| Labeler Name: | Zee Medical Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120612 |
| Package NDC: | 35418-119-37 |
| Package Description: | 6 PACKET in 1 CARTON (35418-119-37) > 10 mL in 1 PACKET (35418-119-42) |
| NDC Code | 35418-119-37 |
| Proprietary Name | Cough Syrup DM |
| Package Description | 6 PACKET in 1 CARTON (35418-119-37) > 10 mL in 1 PACKET (35418-119-42) |
| Product NDC | 35418-119 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin, Dextromethorpham HBr |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20120612 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Zee Medical Inc |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 10; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |