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Mucus Relief - 0363-0532-52 - (Guaifenesin)

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Drug Information of Mucus Relief

Product NDC: 0363-0532
Proprietary Name: Mucus Relief
Non Proprietary Name: Guaifenesin
Active Ingredient(s): 400    mg/1 & nbsp;   Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Mucus Relief

Product NDC: 0363-0532
Labeler Name: WALGREEN CO.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20051222

Package Information of Mucus Relief

Package NDC: 0363-0532-52
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0363-0532-52) > 90 TABLET in 1 BOTTLE, PLASTIC

NDC Information of Mucus Relief

NDC Code 0363-0532-52
Proprietary Name Mucus Relief
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0363-0532-52) > 90 TABLET in 1 BOTTLE, PLASTIC
Product NDC 0363-0532
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20051222
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name WALGREEN CO.
Substance Name GUAIFENESIN
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mucus Relief


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