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Mediflex
Mediflex - 67662-001-03 - (Menthol)
Drug Information of Mediflex
| Product NDC: | 67662-001 |
| Proprietary Name: | Mediflex |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 5 1/85g & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mediflex
| Product NDC: | 67662-001 |
| Labeler Name: | SAS Group Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100329 |
Package Information of Mediflex
| Package NDC: | 67662-001-03 |
| Package Description: | 85 g in 1 JAR (67662-001-03) |
NDC Information of Mediflex
| NDC Code | 67662-001-03 |
| Proprietary Name | Mediflex |
| Package Description | 85 g in 1 JAR (67662-001-03) |
| Product NDC | 67662-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100329 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | SAS Group Inc. |
| Substance Name | MENTHOL |
| Strength Number | 5 |
| Strength Unit | 1/85g |
| Pharmaceutical Classes |
