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cold relief - 41250-014-62 - (Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride)

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Drug Information of cold relief

Product NDC: 41250-014
Proprietary Name: cold relief
Non Proprietary Name: Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Active Ingredient(s): 325; 2; 10; 5    mg/1; mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Chlorpheniramine Maleate, 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: 41250-014
Labeler Name: Meijer Distribution Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20070831

Package Information of cold relief

Package NDC: 41250-014-62
Package Description: 2 BLISTER PACK in 1 CARTON (41250-014-62) > 12 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of cold relief

NDC Code 41250-014-62
Proprietary Name cold relief
Package Description 2 BLISTER PACK in 1 CARTON (41250-014-62) > 12 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 41250-014
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070831
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Meijer Distribution Inc
Substance Name ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 2; 10; 5
Strength Unit mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of cold relief


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