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WellPatch Backache Pain Relief
WellPatch Backache Pain Relief - 10742-8123-2 - (Menthol)
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: | 10742-8123-2 |
| Package Description: | 3 PATCH in 1 POUCH (10742-8123-2) |
NDC Information of WellPatch Backache Pain Relief
| NDC Code | 10742-8123-2 |
| Proprietary Name | WellPatch Backache Pain Relief |
| Package Description | 3 PATCH in 1 POUCH (10742-8123-2) |
| 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 |
