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QuickFlex
QuickFlex - 10056-135-01 - (Menthol)
Drug Information of QuickFlex
| Product NDC: | 10056-135 |
| Proprietary Name: | QuickFlex |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 1.25 g/100g & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of QuickFlex
| Product NDC: | 10056-135 |
| Labeler Name: | Access Business Group International LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100530 |
Package Information of QuickFlex
| Package NDC: | 10056-135-01 |
| Package Description: | 85 g in 1 TUBE (10056-135-01) |
NDC Information of QuickFlex
| NDC Code | 10056-135-01 |
| Proprietary Name | QuickFlex |
| Package Description | 85 g in 1 TUBE (10056-135-01) |
| Product NDC | 10056-135 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100530 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Access Business Group International LLC |
| Substance Name | MENTHOL |
| Strength Number | 1.25 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
