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Up and Up Cold Flu Relief - 11673-215-62 - (Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride)

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Drug Information of Up and Up Cold Flu Relief

Product NDC: 11673-215
Proprietary Name: Up and Up Cold Flu Relief
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Active Ingredient(s): 325; 10; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Up and Up Cold Flu Relief

Product NDC: 11673-215
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100805

Package Information of Up and Up Cold Flu Relief

Package NDC: 11673-215-62
Package Description: 2 BLISTER PACK in 1 CARTON (11673-215-62) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Up and Up Cold Flu Relief

NDC Code 11673-215-62
Proprietary Name Up and Up Cold Flu Relief
Package Description 2 BLISTER PACK in 1 CARTON (11673-215-62) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 11673-215
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20100805
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/1; mg/1; mg/1
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Complete Information of Up and Up Cold Flu Relief


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