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Up and Up Cold Flu Relief - 11673-656-40 - (acetaminophen, dextromethorphan Hbr, Phenylephrine HCl)

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Drug Information of Up and Up Cold Flu Relief

Product NDC: 11673-656
Proprietary Name: Up and Up Cold Flu Relief
Non Proprietary Name: acetaminophen, dextromethorphan Hbr, Phenylephrine HCl
Active Ingredient(s): 325; 10; 5    mg/15mL; mg/15mL; mg/15mL & nbsp;   acetaminophen, dextromethorphan Hbr, Phenylephrine HCl
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: 11673-656
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090707

Package Information of Up and Up Cold Flu Relief

Package NDC: 11673-656-40
Package Description: 355 mL in 1 BOTTLE (11673-656-40)

NDC Information of Up and Up Cold Flu Relief

NDC Code 11673-656-40
Proprietary Name Up and Up Cold Flu Relief
Package Description 355 mL in 1 BOTTLE (11673-656-40)
Product NDC 11673-656
Product Type Name HUMAN OTC DRUG
Non Proprietary Name acetaminophen, dextromethorphan Hbr, Phenylephrine HCl
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090707
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Target Corporation
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 5
Strength Unit mg/15mL; mg/15mL; mg/15mL
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Complete Information of Up and Up Cold Flu Relief


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