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severe cold - 56062-234-62 - (Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl)

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Drug Information of severe cold

Product NDC: 56062-234
Proprietary Name: severe cold
Non Proprietary Name: Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
Active Ingredient(s): 325; 10; 200; 5    mg/1; mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of severe cold

Product NDC: 56062-234
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20071025

Package Information of severe cold

Package NDC: 56062-234-62
Package Description: 2 BLISTER PACK in 1 CARTON (56062-234-62) > 12 TABLET, COATED in 1 BLISTER PACK

NDC Information of severe cold

NDC Code 56062-234-62
Proprietary Name severe cold
Package Description 2 BLISTER PACK in 1 CARTON (56062-234-62) > 12 TABLET, COATED in 1 BLISTER PACK
Product NDC 56062-234
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20071025
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Publix Super Markets Inc
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 10; 200; 5
Strength Unit mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of severe cold


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