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Childrens Mucinex - 63824-017-64 - (acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride)

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Drug Information of Childrens Mucinex

Product NDC: 63824-017
Proprietary Name: Childrens Mucinex
Non Proprietary Name: acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Active Ingredient(s): 650; 20; 400; 10    mg/20mL; mg/20mL; mg/20mL; mg/20mL & nbsp;   acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Childrens Mucinex

Product NDC: 63824-017
Labeler Name: Reckitt Benckiser LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110404

Package Information of Childrens Mucinex

Package NDC: 63824-017-64
Package Description: 1 BOTTLE in 1 CARTON (63824-017-64) > 118 mL in 1 BOTTLE

NDC Information of Childrens Mucinex

NDC Code 63824-017-64
Proprietary Name Childrens Mucinex
Package Description 1 BOTTLE in 1 CARTON (63824-017-64) > 118 mL in 1 BOTTLE
Product NDC 63824-017
Product Type Name HUMAN OTC DRUG
Non Proprietary Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20110404
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Reckitt Benckiser LLC
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 650; 20; 400; 10
Strength Unit mg/20mL; mg/20mL; mg/20mL; mg/20mL
Pharmaceutical Classes

Complete Information of Childrens Mucinex


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