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Arthritis Plus Gel
Arthritis Plus Gel - 50810-2000-1 - (Camphor, Menthol, Methyl Salicylate)
Drug Information of Arthritis Plus Gel
| Product NDC: | 50810-2000 |
| Proprietary Name: | Arthritis Plus Gel |
| Non Proprietary Name: | Camphor, Menthol, Methyl Salicylate |
| Active Ingredient(s): | 3; 12; 15 mg/100mg; mg/100mg; mg/100mg & nbsp; Camphor, Menthol, Methyl Salicylate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arthritis Plus Gel
| Product NDC: | 50810-2000 |
| Labeler Name: | JI Well Health Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130701 |
Package Information of Arthritis Plus Gel
| Package NDC: | 50810-2000-1 |
| Package Description: | 1 TUBE in 1 BOX (50810-2000-1) > 57 mg in 1 TUBE |
NDC Information of Arthritis Plus Gel
| NDC Code | 50810-2000-1 |
| Proprietary Name | Arthritis Plus Gel |
| Package Description | 1 TUBE in 1 BOX (50810-2000-1) > 57 mg in 1 TUBE |
| Product NDC | 50810-2000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Camphor, Menthol, Methyl Salicylate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130701 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | JI Well Health Company |
| Substance Name | CAMPHOR (NATURAL); MENTHOL; METHYL SALICYLATE |
| Strength Number | 3; 12; 15 |
| Strength Unit | mg/100mg; mg/100mg; mg/100mg |
| Pharmaceutical Classes |
