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Sinus Headache - 59779-502-07 - (Acetaminophen and Phenylephrine HCl)

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Drug Information of Sinus Headache

Product NDC: 59779-502
Proprietary Name: Sinus Headache
Non Proprietary Name: Acetaminophen and Phenylephrine HCl
Active Ingredient(s): 325; 5    mg/1; mg/1 & nbsp;   Acetaminophen and Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sinus Headache

Product NDC: 59779-502
Labeler Name: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20050623

Package Information of Sinus Headache

Package NDC: 59779-502-07
Package Description: 1 BLISTER PACK in 1 CARTON (59779-502-07) > 36 TABLET in 1 BLISTER PACK

NDC Information of Sinus Headache

NDC Code 59779-502-07
Proprietary Name Sinus Headache
Package Description 1 BLISTER PACK in 1 CARTON (59779-502-07) > 36 TABLET in 1 BLISTER PACK
Product NDC 59779-502
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and Phenylephrine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050623
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Substance Name ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Sinus Headache


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