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Terocin
Terocin - 50488-1001-1 - (Lidocaine, Menthol)
Drug Information of Terocin
| Product NDC: | 50488-1001 |
| Proprietary Name: | Terocin |
| Non Proprietary Name: | Lidocaine, Menthol |
| Active Ingredient(s): | 600; 600 mg/1; mg/1 & nbsp; Lidocaine, Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | PATCH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Terocin
| Product NDC: | 50488-1001 |
| Labeler Name: | Alexso Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130501 |
Package Information of Terocin
| Package NDC: | 50488-1001-1 |
| Package Description: | 2 POUCH in 1 BOX (50488-1001-1) > 5 PATCH in 1 POUCH |
NDC Information of Terocin
| NDC Code | 50488-1001-1 |
| Proprietary Name | Terocin |
| Package Description | 2 POUCH in 1 BOX (50488-1001-1) > 5 PATCH in 1 POUCH |
| Product NDC | 50488-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Lidocaine, Menthol |
| Dosage Form Name | PATCH |
| Route Name | TOPICAL |
| Start Marketing Date | 20130501 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Alexso Inc. |
| Substance Name | LIDOCAINE; MENTHOL |
| Strength Number | 600; 600 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
