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Sinus Congestion and Pain Severe Daytime - 0363-5270-08 - (Aceetaminophen, Guaifenesin and Phenylephrine HCl)

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Drug Information of Sinus Congestion and Pain Severe Daytime

Product NDC: 0363-5270
Proprietary Name: Sinus Congestion and Pain Severe Daytime
Non Proprietary Name: Aceetaminophen, Guaifenesin and Phenylephrine HCl
Active Ingredient(s): 325; 200; 5    mg/1; mg/1; mg/1 & nbsp;   Aceetaminophen, Guaifenesin and Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sinus Congestion and Pain Severe Daytime

Product NDC: 0363-5270
Labeler Name: WALGREEN CO.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20050806

Package Information of Sinus Congestion and Pain Severe Daytime

Package NDC: 0363-5270-08
Package Description: 2 BLISTER PACK in 1 CARTON (0363-5270-08) > 12 TABLET in 1 BLISTER PACK

NDC Information of Sinus Congestion and Pain Severe Daytime

NDC Code 0363-5270-08
Proprietary Name Sinus Congestion and Pain Severe Daytime
Package Description 2 BLISTER PACK in 1 CARTON (0363-5270-08) > 12 TABLET in 1 BLISTER PACK
Product NDC 0363-5270
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Aceetaminophen, Guaifenesin and Phenylephrine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050806
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name WALGREEN CO.
Substance Name ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 200; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Sinus Congestion and Pain Severe Daytime


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