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 |