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MyoRx
MyoRx - 59088-962-05 - (Menthol)
Drug Information of MyoRx
| Product NDC: | 59088-962 |
| Proprietary Name: | MyoRx |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 20 uL/mL & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MyoRx
| Product NDC: | 59088-962 |
| Labeler Name: | PureTek Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100128 |
Package Information of MyoRx
| Package NDC: | 59088-962-05 |
| Package Description: | 59 mL in 1 JAR (59088-962-05) |
NDC Information of MyoRx
| NDC Code | 59088-962-05 |
| Proprietary Name | MyoRx |
| Package Description | 59 mL in 1 JAR (59088-962-05) |
| Product NDC | 59088-962 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100128 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | PureTek Corporation |
| Substance Name | MENTHOL |
| Strength Number | 20 |
| Strength Unit | uL/mL |
| Pharmaceutical Classes |
