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TYLENOL SINUS - 50580-262-02 - (Acetaminophen, Guaifenesin, and Phenylephrine hydrochloride)

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Drug Information of TYLENOL SINUS

Product NDC: 50580-262
Proprietary Name: TYLENOL SINUS
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of TYLENOL SINUS

Product NDC: 50580-262
Labeler Name: McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060301

Package Information of TYLENOL SINUS

Package NDC: 50580-262-02
Package Description: 2 TABLET, FILM COATED in 1 POUCH (50580-262-02)

NDC Information of TYLENOL SINUS

NDC Code 50580-262-02
Proprietary Name TYLENOL SINUS
Package Description 2 TABLET, FILM COATED in 1 POUCH (50580-262-02)
Product NDC 50580-262
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Guaifenesin, and Phenylephrine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060301
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Substance Name ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 200; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of TYLENOL SINUS


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