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Cold Relief - 59779-402-62 - (Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride)

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Drug Information of Cold Relief

Product NDC: 59779-402
Proprietary Name: Cold Relief
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Active Ingredient(s): 325; 10; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Cold Relief

Product NDC: 59779-402
Labeler Name: CVS Pharmacy
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090612

Package Information of Cold Relief

Package NDC: 59779-402-62
Package Description: 2 BLISTER PACK in 1 CARTON (59779-402-62) > 12 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Cold Relief

NDC Code 59779-402-62
Proprietary Name Cold Relief
Package Description 2 BLISTER PACK in 1 CARTON (59779-402-62) > 12 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 59779-402
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090612
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name CVS Pharmacy
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Cold Relief


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