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up and up cold and flu relief - 11673-335-40 - (Acetaminophen, Dextromethorphan HBr, Doxylamine succinate)

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Drug Information of up and up cold and flu relief

Product NDC: 11673-335
Proprietary Name: up and up cold and flu relief
Non Proprietary Name: Acetaminophen, Dextromethorphan HBr, Doxylamine succinate
Active Ingredient(s): 650; 30; 12.5    mg/30mL; mg/30mL; mg/30mL & 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 and flu relief

Product NDC: 11673-335
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110923

Package Information of up and up cold and flu relief

Package NDC: 11673-335-40
Package Description: 355 mL in 1 BOTTLE (11673-335-40)

NDC Information of up and up cold and flu relief

NDC Code 11673-335-40
Proprietary Name up and up cold and flu relief
Package Description 355 mL in 1 BOTTLE (11673-335-40)
Product NDC 11673-335
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan HBr, Doxylamine succinate
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20110923
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Target Corporation
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE
Strength Number 650; 30; 12.5
Strength Unit mg/30mL; mg/30mL; mg/30mL
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Complete Information of up and up cold and flu relief


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