| Product NDC: | 44924-101 |
| Proprietary Name: | High Protection Sun SPF 30 |
| Non Proprietary Name: | Titanium Dioxide |
| Active Ingredient(s): | 15; 15.5 mL/200mL; mL/200mL & nbsp; Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 44924-101 |
| Labeler Name: | Babor Cosmetics America, Corp. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100301 |
| Package NDC: | 44924-101-02 |
| Package Description: | 1 TUBE in 1 CARTON (44924-101-02) > 200 mL in 1 TUBE (44924-101-01) |
| NDC Code | 44924-101-02 |
| Proprietary Name | High Protection Sun SPF 30 |
| Package Description | 1 TUBE in 1 CARTON (44924-101-02) > 200 mL in 1 TUBE (44924-101-01) |
| Product NDC | 44924-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium Dioxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Babor Cosmetics America, Corp. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 15; 15.5 |
| Strength Unit | mL/200mL; mL/200mL |
| Pharmaceutical Classes |