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Regemarine
Regemarine - 42248-112-01 - (OCTINOXATE)
Drug Information of Regemarine
| Product NDC: | 42248-112 |
| Proprietary Name: | Regemarine |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 15 mL/200mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Regemarine
| Product NDC: | 42248-112 |
| Labeler Name: | Zenith Medicosm SL |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110815 |
Package Information of Regemarine
| Package NDC: | 42248-112-01 |
| Package Description: | 200 mL in 1 TUBE (42248-112-01) |
NDC Information of Regemarine
| NDC Code | 42248-112-01 |
| Proprietary Name | Regemarine |
| Package Description | 200 mL in 1 TUBE (42248-112-01) |
| Product NDC | 42248-112 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110815 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Zenith Medicosm SL |
| Substance Name | OCTINOXATE |
| Strength Number | 15 |
| Strength Unit | mL/200mL |
| Pharmaceutical Classes |
