| Product NDC: | 0031-8713 |
| Proprietary Name: | ROBITUSSIN TO GO COUGH AND COLD CF |
| Non Proprietary Name: | dextromethorphan HBr, guaifenesin, phenylephrine HCl |
| Active Ingredient(s): | 20; 200; 10 mg/10mL; mg/10mL; mg/10mL & nbsp; dextromethorphan HBr, guaifenesin, phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0031-8713 |
| Labeler Name: | Richmond Division of Wyeth |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080107 |
| Package NDC: | 0031-8713-10 |
| Package Description: | 10 POUCH in 1 CARTON (0031-8713-10) > 1 VIAL, SINGLE-DOSE in 1 POUCH > 10 mL in 1 VIAL, SINGLE-DOSE |
| NDC Code | 0031-8713-10 |
| Proprietary Name | ROBITUSSIN TO GO COUGH AND COLD CF |
| Package Description | 10 POUCH in 1 CARTON (0031-8713-10) > 1 VIAL, SINGLE-DOSE in 1 POUCH > 10 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0031-8713 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dextromethorphan HBr, guaifenesin, phenylephrine HCl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20080107 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Richmond Division of Wyeth |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 20; 200; 10 |
| Strength Unit | mg/10mL; mg/10mL; mg/10mL |
| Pharmaceutical Classes |