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WellPatch Backache Pain Relief - 10742-8123-1 - (Menthol)

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Drug Information of WellPatch Backache Pain Relief

Product NDC: 10742-8123
Proprietary Name: WellPatch Backache Pain Relief
Non Proprietary Name: Menthol
Active Ingredient(s): 50    mg/1 & nbsp;   Menthol
Administration Route(s): TOPICAL
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of WellPatch Backache Pain Relief

Product NDC: 10742-8123
Labeler Name: The Mentholatum Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20080118

Package Information of WellPatch Backache Pain Relief

Package NDC: 10742-8123-1
Package Description: 1 POUCH in 1 CARTON (10742-8123-1) > 4 PATCH in 1 POUCH

NDC Information of WellPatch Backache Pain Relief

NDC Code 10742-8123-1
Proprietary Name WellPatch Backache Pain Relief
Package Description 1 POUCH in 1 CARTON (10742-8123-1) > 4 PATCH in 1 POUCH
Product NDC 10742-8123
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Menthol
Dosage Form Name PATCH
Route Name TOPICAL
Start Marketing Date 20080118
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name The Mentholatum Company
Substance Name MENTHOL
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of WellPatch Backache Pain Relief


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