Product NDC: | 76446-004 |
Proprietary Name: | ANNA LOTAN Rejuvenating Day Broad Spectrum SPF 34 |
Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE |
Active Ingredient(s): | 7.5; 4.4 mL/100mL; mL/100mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76446-004 |
Labeler Name: | Anna Lotan Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120619 |
Package NDC: | 76446-004-75 |
Package Description: | 75 mL in 1 BOTTLE (76446-004-75) |
NDC Code | 76446-004-75 |
Proprietary Name | ANNA LOTAN Rejuvenating Day Broad Spectrum SPF 34 |
Package Description | 75 mL in 1 BOTTLE (76446-004-75) |
Product NDC | 76446-004 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120619 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Anna Lotan Ltd |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 7.5; 4.4 |
Strength Unit | mL/100mL; mL/100mL |
Pharmaceutical Classes |