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Mucus Relief PE - 0363-0542-01 - (Guaifenesin, Phenylephrine HCl)

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Drug Information of Mucus Relief PE

Product NDC: 0363-0542
Proprietary Name: Mucus Relief PE
Non Proprietary Name: Guaifenesin, Phenylephrine HCl
Active Ingredient(s): 400; 10    mg/1; mg/1 & nbsp;   Guaifenesin, Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Mucus Relief PE

Product NDC: 0363-0542
Labeler Name: Walgreen Co.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060415

Package Information of Mucus Relief PE

Package NDC: 0363-0542-01
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0363-0542-01) > 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of Mucus Relief PE

NDC Code 0363-0542-01
Proprietary Name Mucus Relief PE
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0363-0542-01) > 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 0363-0542
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin, Phenylephrine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060415
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Walgreen Co.
Substance Name GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 400; 10
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Mucus Relief PE


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