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Night Relief sinus - 55312-101-16 - (Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride)

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Drug Information of Night Relief sinus

Product NDC: 55312-101
Proprietary Name: Night Relief sinus
Non Proprietary Name: Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride
Active Ingredient(s): 325; 6.25; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Night Relief sinus

Product NDC: 55312-101
Labeler Name: Western Family Foods, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120712

Package Information of Night Relief sinus

Package NDC: 55312-101-16
Package Description: 2 BLISTER PACK in 1 CARTON (55312-101-16) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Night Relief sinus

NDC Code 55312-101-16
Proprietary Name Night Relief sinus
Package Description 2 BLISTER PACK in 1 CARTON (55312-101-16) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 55312-101
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Doxylamine succinate and Phenylephrine Hydrochloride
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120712
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Western Family Foods, Inc.
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 Night Relief sinus


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