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Arthritis Relief - 50972-272-01 - (Menthol)

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Drug Information of Arthritis Relief

Product NDC: 50972-272
Proprietary Name: Arthritis Relief
Non Proprietary Name: Menthol
Active Ingredient(s): 12.5    mg/g & nbsp;   Menthol
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Arthritis Relief

Product NDC: 50972-272
Labeler Name: NewMarket Health Products LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120413

Package Information of Arthritis Relief

Package NDC: 50972-272-01
Package Description: 57 g in 1 TUBE (50972-272-01)

NDC Information of Arthritis Relief

NDC Code 50972-272-01
Proprietary Name Arthritis Relief
Package Description 57 g in 1 TUBE (50972-272-01)
Product NDC 50972-272
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Menthol
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120413
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name NewMarket Health Products LLC
Substance Name MENTHOL
Strength Number 12.5
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Arthritis Relief


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