| Product NDC: | 44924-123 |
| Proprietary Name: | Derma Refiner Day |
| Non Proprietary Name: | Octinoxate |
| Active Ingredient(s): | 2.5; 2; 2 mL/50mL; mL/50mL; mL/50mL & nbsp; Octinoxate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 44924-123 |
| Labeler Name: | Babor Cosmetics America, Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090615 |
| Package NDC: | 44924-123-02 |
| Package Description: | 1 JAR in 1 BOX (44924-123-02) > 50 mL in 1 JAR (44924-123-01) |
| NDC Code | 44924-123-02 |
| Proprietary Name | Derma Refiner Day |
| Package Description | 1 JAR in 1 BOX (44924-123-02) > 50 mL in 1 JAR (44924-123-01) |
| Product NDC | 44924-123 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090615 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Babor Cosmetics America, Corp |
| Substance Name | OCTINOXATE; OCTOCRYLENE; TITANIUM DIOXIDE |
| Strength Number | 2.5; 2; 2 |
| Strength Unit | mL/50mL; mL/50mL; mL/50mL |
| Pharmaceutical Classes |