Product NDC: | 57900-001 |
Proprietary Name: | Assured |
Non Proprietary Name: | DL-Camphor L-Menthol Methyl Salicylate |
Active Ingredient(s): | 1.2; 5.7; 6.3 mg/100mg; mg/100mg; mg/100mg & nbsp; DL-Camphor L-Menthol Methyl Salicylate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | PATCH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57900-001 |
Labeler Name: | Zhejiang Bangli Medical Products Co., Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130501 |
Package NDC: | 57900-001-01 |
Package Description: | 2000 mg in 1 BOX (57900-001-01) |
NDC Code | 57900-001-01 |
Proprietary Name | Assured |
Package Description | 2000 mg in 1 BOX (57900-001-01) |
Product NDC | 57900-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DL-Camphor L-Menthol Methyl Salicylate |
Dosage Form Name | PATCH |
Route Name | TOPICAL |
Start Marketing Date | 20130501 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Zhejiang Bangli Medical Products Co., Ltd |
Substance Name | CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE |
Strength Number | 1.2; 5.7; 6.3 |
Strength Unit | mg/100mg; mg/100mg; mg/100mg |
Pharmaceutical Classes |