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