CounterAct - 54473-185-36 - (Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine)

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Drug Information of CounterAct

Product NDC: 54473-185
Proprietary Name: CounterAct
Non Proprietary Name: Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine
Active Ingredient(s): 325; 10; 200; 5    mg/1; mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of CounterAct

Product NDC: 54473-185
Labeler Name: Melaleuca, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20111001

Package Information of CounterAct

Package NDC: 54473-185-36
Package Description: 3 BLISTER PACK in 1 BOX (54473-185-36) > 12 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of CounterAct

NDC Code 54473-185-36
Proprietary Name CounterAct
Package Description 3 BLISTER PACK in 1 BOX (54473-185-36) > 12 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 54473-185
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111001
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Melaleuca, 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 CounterAct


General Information