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 |