cold - 30142-308-62 - (Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride)

Alphabetical Index


Drug Information of cold

Product NDC: 30142-308
Proprietary Name: cold
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Active Ingredient(s): 325; 10; 200; 5    mg/1; mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of cold

Product NDC: 30142-308
Labeler Name: Kroger Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20080820

Package Information of cold

Package NDC: 30142-308-62
Package Description: 2 BLISTER PACK in 1 CARTON (30142-308-62) > 12 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of cold

NDC Code 30142-308-62
Proprietary Name cold
Package Description 2 BLISTER PACK in 1 CARTON (30142-308-62) > 12 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 30142-308
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080820
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Kroger Company
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 cold


General Information