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DayTime Cold and Flu - 53345-004-01 - (acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride)

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Drug Information of DayTime Cold and Flu

Product NDC: 53345-004
Proprietary Name: DayTime Cold and Flu
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 DayTime Cold and Flu

Product NDC: 53345-004
Labeler Name: Humanwell PuraCap Pharmaceutical (Wuhan), Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130615

Package Information of DayTime Cold and Flu

Package NDC: 53345-004-01
Package Description: 1 BAG in 1 BOX (53345-004-01) > 4000 CAPSULE, LIQUID FILLED in 1 BAG

NDC Information of DayTime Cold and Flu

NDC Code 53345-004-01
Proprietary Name DayTime Cold and Flu
Package Description 1 BAG in 1 BOX (53345-004-01) > 4000 CAPSULE, LIQUID FILLED in 1 BAG
Product NDC 53345-004
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 20130615
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Humanwell PuraCap Pharmaceutical (Wuhan), Ltd.
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of DayTime Cold and Flu


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