Home
>
National Drug Code (NDC)
>
up and up tussin multi symptom cold
up and up tussin multi symptom cold - 11673-296-26 - (dextromethorphan hbr, guaifenesin, phenylephrine hcl)
Drug Information of up and up tussin multi symptom cold
| Product NDC: | 11673-296 |
| Proprietary Name: | up and up tussin multi symptom cold |
| Non Proprietary Name: | dextromethorphan hbr, guaifenesin, phenylephrine hcl |
| Active Ingredient(s): | 10; 200; 5 mg/5mL; mg/5mL; mg/5mL & nbsp; dextromethorphan hbr, guaifenesin, phenylephrine hcl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of up and up tussin multi symptom cold
| Product NDC: | 11673-296 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121217 |
Package Information of up and up tussin multi symptom cold
| Package NDC: | 11673-296-26 |
| Package Description: | 1 BOTTLE in 1 CARTON (11673-296-26) > 118 mL in 1 BOTTLE |
NDC Information of up and up tussin multi symptom cold
| NDC Code | 11673-296-26 |
| Proprietary Name | up and up tussin multi symptom cold |
| Package Description | 1 BOTTLE in 1 CARTON (11673-296-26) > 118 mL in 1 BOTTLE |
| Product NDC | 11673-296 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dextromethorphan hbr, guaifenesin, phenylephrine hcl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20121217 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Target Corporation |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10; 200; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
