| Product NDC: | 0363-0934 |
| Proprietary Name: | wal tussin dm max |
| Non Proprietary Name: | dextromethorphan hbr, guaifenesin |
| Active Ingredient(s): | 10; 200 mg/5mL; mg/5mL & nbsp; dextromethorphan hbr, guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0363-0934 |
| Labeler Name: | Walgreen Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120119 |
| Package NDC: | 0363-0934-26 |
| Package Description: | 1 BOTTLE in 1 CARTON (0363-0934-26) > 118 mL in 1 BOTTLE |
| NDC Code | 0363-0934-26 |
| Proprietary Name | wal tussin dm max |
| Package Description | 1 BOTTLE in 1 CARTON (0363-0934-26) > 118 mL in 1 BOTTLE |
| Product NDC | 0363-0934 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dextromethorphan hbr, guaifenesin |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120119 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Walgreen Company |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 10; 200 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |