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Neutrogena Intensified Day Moisture
Neutrogena Intensified Day Moisture - 10812-907-02 - (Ensulizole and Octinoxate)
Drug Information of Neutrogena Intensified Day Moisture
| Product NDC: | 10812-907 |
| Proprietary Name: | Neutrogena Intensified Day Moisture |
| Non Proprietary Name: | Ensulizole and Octinoxate |
| Active Ingredient(s): | 10; 75 mg/g; mg/g & nbsp; Ensulizole and Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Neutrogena Intensified Day Moisture
| Product NDC: | 10812-907 |
| Labeler Name: | Neutrogena Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100601 |
Package Information of Neutrogena Intensified Day Moisture
| Package NDC: | 10812-907-02 |
| Package Description: | 1 JAR in 1 CARTON (10812-907-02) > 63 g in 1 JAR |
NDC Information of Neutrogena Intensified Day Moisture
| NDC Code | 10812-907-02 |
| Proprietary Name | Neutrogena Intensified Day Moisture |
| Package Description | 1 JAR in 1 CARTON (10812-907-02) > 63 g in 1 JAR |
| Product NDC | 10812-907 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ensulizole and Octinoxate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Neutrogena Corporation |
| Substance Name | ENSULIZOLE; OCTINOXATE |
| Strength Number | 10; 75 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
