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Day relief sinus PE - 55312-100-12 - (Acetaminophen and Phenylephrine Hydrochloride)

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Drug Information of Day relief sinus PE

Product NDC: 55312-100
Proprietary Name: Day relief sinus PE
Non Proprietary Name: Acetaminophen and Phenylephrine Hydrochloride
Active Ingredient(s): 325; 5    mg/1; mg/1 & nbsp;   Acetaminophen and Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Day relief sinus PE

Product NDC: 55312-100
Labeler Name: Western Family Foods, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120710

Package Information of Day relief sinus PE

Package NDC: 55312-100-12
Package Description: 1 BLISTER PACK in 1 CARTON (55312-100-12) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Day relief sinus PE

NDC Code 55312-100-12
Proprietary Name Day relief sinus PE
Package Description 1 BLISTER PACK in 1 CARTON (55312-100-12) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 55312-100
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and Phenylephrine Hydrochloride
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120710
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Western Family Foods, Inc.
Substance Name ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Day relief sinus PE


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