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Allergy Relief - 59779-559-08 - (Acetaminophen, Phenylephrine HCl, Chlorpheniramine maleate)

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Drug Information of Allergy Relief

Product NDC: 59779-559
Proprietary Name: Allergy Relief
Non Proprietary Name: Acetaminophen, Phenylephrine HCl, Chlorpheniramine maleate
Active Ingredient(s): 325; 2; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Phenylephrine HCl, Chlorpheniramine maleate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Allergy Relief

Product NDC: 59779-559
Labeler Name: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20080317

Package Information of Allergy Relief

Package NDC: 59779-559-08
Package Description: 1 BLISTER PACK in 1 CARTON (59779-559-08) > 24 CAPSULE, GELATIN COATED in 1 BLISTER PACK

NDC Information of Allergy Relief

NDC Code 59779-559-08
Proprietary Name Allergy Relief
Package Description 1 BLISTER PACK in 1 CARTON (59779-559-08) > 24 CAPSULE, GELATIN COATED in 1 BLISTER PACK
Product NDC 59779-559
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Phenylephrine HCl, Chlorpheniramine maleate
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20080317
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Substance Name ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 2; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Allergy Relief


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