| Product NDC: | 43458-1003 |
| Proprietary Name: | Vertra SPF 50 Foundation Sunscreen Face Translucent |
| Non Proprietary Name: | TITANIUM DIOXIDE, PADIMATE O |
| Active Ingredient(s): | 7; 17.4 g/100g; g/100g & nbsp; TITANIUM DIOXIDE, PADIMATE O |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43458-1003 |
| Labeler Name: | Vertra, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120708 |
| Package NDC: | 43458-1003-9 |
| Package Description: | 10.5 g in 1 DIALPACK (43458-1003-9) |
| NDC Code | 43458-1003-9 |
| Proprietary Name | Vertra SPF 50 Foundation Sunscreen Face Translucent |
| Package Description | 10.5 g in 1 DIALPACK (43458-1003-9) |
| Product NDC | 43458-1003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE, PADIMATE O |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20120708 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Vertra, Inc |
| Substance Name | PADIMATE O; TITANIUM DIOXIDE |
| Strength Number | 7; 17.4 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |