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Up and Up Cold Flu Relief
Up and Up Cold Flu Relief - 11673-908-38 - (acetaminophen,dextromethorphan HBr, doxylamine succinate)
Drug Information of Up and Up Cold Flu Relief
| Product NDC: | 11673-908 |
| Proprietary Name: | Up and Up Cold Flu Relief |
| Non Proprietary Name: | acetaminophen,dextromethorphan HBr, doxylamine succinate |
| Active Ingredient(s): | 500; 15; 6.25 mg/15mL; mg/15mL; mg/15mL & nbsp; acetaminophen,dextromethorphan HBr, doxylamine succinate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Up and Up Cold Flu Relief
| Product NDC: | 11673-908 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090611 |
Package Information of Up and Up Cold Flu Relief
| Package NDC: | 11673-908-38 |
| Package Description: | 295 mL in 1 BOTTLE (11673-908-38) |
NDC Information of Up and Up Cold Flu Relief
| NDC Code | 11673-908-38 |
| Proprietary Name | Up and Up Cold Flu Relief |
| Package Description | 295 mL in 1 BOTTLE (11673-908-38) |
| Product NDC | 11673-908 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen,dextromethorphan HBr, doxylamine succinate |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20090611 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Target Corporation |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 500; 15; 6.25 |
| Strength Unit | mg/15mL; mg/15mL; mg/15mL |
| Pharmaceutical Classes |
