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up and up cold relief - 11673-250-56 - (Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl)

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Drug Information of up and up cold relief

Product NDC: 11673-250
Proprietary Name: up and up cold relief
Non Proprietary Name: Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl
Active Ingredient(s):    & nbsp;   Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of up and up cold relief

Product NDC: 11673-250
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090731

Package Information of up and up cold relief

Package NDC: 11673-250-56
Package Description: 1 KIT in 1 CARTON (11673-250-56) * 12 TABLET, FILM COATED in 1 BLISTER PACK * 8 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of up and up cold relief

NDC Code 11673-250-56
Proprietary Name up and up cold relief
Package Description 1 KIT in 1 CARTON (11673-250-56) * 12 TABLET, FILM COATED in 1 BLISTER PACK * 8 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 11673-250
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl
Dosage Form Name KIT
Route Name
Start Marketing Date 20090731
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Target Corporation
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of up and up cold relief


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