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Panitrol
Panitrol - 59940-001-03 - (Menthol)
Drug Information of Panitrol
| Product NDC: | 59940-001 |
| Proprietary Name: | Panitrol |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 4.25 g/85g & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Panitrol
| Product NDC: | 59940-001 |
| Labeler Name: | Enzyme Labs |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101101 |
Package Information of Panitrol
| Package NDC: | 59940-001-03 |
| Package Description: | 85 g in 1 TUBE (59940-001-03) |
NDC Information of Panitrol
| NDC Code | 59940-001-03 |
| Proprietary Name | Panitrol |
| Package Description | 85 g in 1 TUBE (59940-001-03) |
| Product NDC | 59940-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Enzyme Labs |
| Substance Name | MENTHOL |
| Strength Number | 4.25 |
| Strength Unit | g/85g |
| Pharmaceutical Classes |
