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Hydromarine
Hydromarine - 42248-101-02 - (OCTINOXATE)
Drug Information of Hydromarine
| Product NDC: | 42248-101 |
| Proprietary Name: | Hydromarine |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | 3.75 mL/50mL & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydromarine
| Product NDC: | 42248-101 |
| 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 Hydromarine
| Package NDC: | 42248-101-02 |
| Package Description: | 1 JAR in 1 BOX (42248-101-02) > 50 mL in 1 JAR |
NDC Information of Hydromarine
| NDC Code | 42248-101-02 |
| Proprietary Name | Hydromarine |
| Package Description | 1 JAR in 1 BOX (42248-101-02) > 50 mL in 1 JAR |
| Product NDC | 42248-101 |
| 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 | 3.75 |
| Strength Unit | mL/50mL |
| Pharmaceutical Classes |
