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Severe Cold Relief PE - 59779-652-07 - (Acetaminophen, Diphenhydramine HCl and Phenylephrine HCl)

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Drug Information of Severe Cold Relief PE

Product NDC: 59779-652
Proprietary Name: Severe Cold Relief PE
Non Proprietary Name: Acetaminophen, Diphenhydramine HCl and Phenylephrine HCl
Active Ingredient(s): 325; 12.5; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Diphenhydramine HCl and Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Severe Cold Relief PE

Product NDC: 59779-652
Labeler Name: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20050621

Package Information of Severe Cold Relief PE

Package NDC: 59779-652-07
Package Description: 1 BLISTER PACK in 1 CARTON (59779-652-07) > 36 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Severe Cold Relief PE

NDC Code 59779-652-07
Proprietary Name Severe Cold Relief PE
Package Description 1 BLISTER PACK in 1 CARTON (59779-652-07) > 36 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 59779-652
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl and Phenylephrine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050621
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 12.5; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Severe Cold Relief PE


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