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Mucinex Sinus-Max - 63824-200-30 - (Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride)

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Drug Information of Mucinex Sinus-Max

Product NDC: 63824-200
Proprietary Name: Mucinex Sinus-Max
Non Proprietary Name: Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride
Active Ingredient(s): 325; 200; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Mucinex Sinus-Max

Product NDC: 63824-200
Labeler Name: Reckitt Benckiser LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120723

Package Information of Mucinex Sinus-Max

Package NDC: 63824-200-30
Package Description: 3 BLISTER PACK in 1 CARTON (63824-200-30) > 10 TABLET, COATED in 1 BLISTER PACK

NDC Information of Mucinex Sinus-Max

NDC Code 63824-200-30
Proprietary Name Mucinex Sinus-Max
Package Description 3 BLISTER PACK in 1 CARTON (63824-200-30) > 10 TABLET, COATED in 1 BLISTER PACK
Product NDC 63824-200
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20120723
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Reckitt Benckiser LLC
Substance Name ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 200; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Mucinex Sinus-Max


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