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Up and Up nasal decongestant PE - 11673-094-89 - (Phenylephrine Hydrochloride)

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Drug Information of Up and Up nasal decongestant PE

Product NDC: 11673-094
Proprietary Name: Up and Up nasal decongestant PE
Non Proprietary Name: Phenylephrine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Up and Up nasal decongestant PE

Product NDC: 11673-094
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090612

Package Information of Up and Up nasal decongestant PE

Package NDC: 11673-094-89
Package Description: 1 BLISTER PACK in 1 CARTON (11673-094-89) > 18 TABLET in 1 BLISTER PACK

NDC Information of Up and Up nasal decongestant PE

NDC Code 11673-094-89
Proprietary Name Up and Up nasal decongestant PE
Package Description 1 BLISTER PACK in 1 CARTON (11673-094-89) > 18 TABLET in 1 BLISTER PACK
Product NDC 11673-094
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Phenylephrine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090612
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Target Corporation
Substance Name PHENYLEPHRINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Up and Up nasal decongestant PE


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