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OsmoFlex
OsmoFlex - 67676-101-01 - (Menthol)
Drug Information of OsmoFlex
| Product NDC: | 67676-101 |
| Proprietary Name: | OsmoFlex |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 1.3 g/100g & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OsmoFlex
| Product NDC: | 67676-101 |
| Labeler Name: | Sarati International, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19930101 |
Package Information of OsmoFlex
| Package NDC: | 67676-101-01 |
| Package Description: | 113.4 g in 1 TUBE (67676-101-01) |
NDC Information of OsmoFlex
| NDC Code | 67676-101-01 |
| Proprietary Name | OsmoFlex |
| Package Description | 113.4 g in 1 TUBE (67676-101-01) |
| Product NDC | 67676-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19930101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sarati International, Inc. |
| Substance Name | MENTHOL |
| Strength Number | 1.3 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
