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up and up flu and severe cold and cough relief
up and up flu and severe cold and cough relief - 11673-964-91 - (Acetaminophen, Diphenhydramine hydrochloride, Phenylephrine hydrochloride)
Drug Information of up and up flu and severe cold and cough relief
| Product NDC: | 11673-964 |
| Proprietary Name: | up and up flu and severe cold and cough relief |
| Non Proprietary Name: | Acetaminophen, Diphenhydramine hydrochloride, Phenylephrine hydrochloride |
| Active Ingredient(s): | 650; 25; 10 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Diphenhydramine hydrochloride, Phenylephrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of up and up flu and severe cold and cough relief
| Product NDC: | 11673-964 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100902 |
Package Information of up and up flu and severe cold and cough relief
| Package NDC: | 11673-964-91 |
| Package Description: | 6 POWDER, FOR SOLUTION in 1 CARTON (11673-964-91) |
NDC Information of up and up flu and severe cold and cough relief
| NDC Code | 11673-964-91 |
| Proprietary Name | up and up flu and severe cold and cough relief |
| Package Description | 6 POWDER, FOR SOLUTION in 1 CARTON (11673-964-91) |
| Product NDC | 11673-964 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Diphenhydramine hydrochloride, Phenylephrine hydrochloride |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20100902 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Target Corporation |
| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 650; 25; 10 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
