| Product NDC: | 76446-002 |
| Proprietary Name: | ANNA LOTAN Premium B.B. UVA UVB SPF 36 |
| Non Proprietary Name: | TITANIUM DIOXIDE, OCTINOXATE |
| Active Ingredient(s): | 15; 30 mL/100mL; mL/100mL & nbsp; TITANIUM DIOXIDE, OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76446-002 |
| Labeler Name: | Anna Lotan Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120616 |
| Package NDC: | 76446-002-30 |
| Package Description: | 30 mL in 1 BOTTLE (76446-002-30) |
| NDC Code | 76446-002-30 |
| Proprietary Name | ANNA LOTAN Premium B.B. UVA UVB SPF 36 |
| Package Description | 30 mL in 1 BOTTLE (76446-002-30) |
| Product NDC | 76446-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE, OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120616 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Anna Lotan Ltd |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 15; 30 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |