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NightTime Sinus Relief - 53345-013-01 - (Acetaminophen, Doxylamine succinate, Phenylephrine hydrochloride)

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Drug Information of NightTime Sinus Relief

Product NDC: 53345-013
Proprietary Name: NightTime Sinus Relief
Non Proprietary Name: Acetaminophen, Doxylamine succinate, Phenylephrine hydrochloride
Active Ingredient(s): 325; 6.25; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Doxylamine succinate, Phenylephrine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of NightTime Sinus Relief

Product NDC: 53345-013
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 NightTime Sinus Relief

Package NDC: 53345-013-01
Package Description: 1 BAG in 1 BOX (53345-013-01) > 4000 CAPSULE, LIQUID FILLED in 1 BAG

NDC Information of NightTime Sinus Relief

NDC Code 53345-013-01
Proprietary Name NightTime Sinus Relief
Package Description 1 BAG in 1 BOX (53345-013-01) > 4000 CAPSULE, LIQUID FILLED in 1 BAG
Product NDC 53345-013
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Doxylamine succinate, 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; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 6.25; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of NightTime Sinus Relief


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