| Product NDC: | 67226-2045 |
| Proprietary Name: | VivierSkin Sun Protection |
| Non Proprietary Name: | ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE |
| Active Ingredient(s): | 7.5; 7.5; 4.8 mL/100mL; mL/100mL; mL/100mL & nbsp; ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67226-2045 |
| Labeler Name: | Vivier Pharma, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110325 |
| Package NDC: | 67226-2045-1 |
| Package Description: | 1 TUBE in 1 BOX (67226-2045-1) > 100 mL in 1 TUBE |
| NDC Code | 67226-2045-1 |
| Proprietary Name | VivierSkin Sun Protection |
| Package Description | 1 TUBE in 1 BOX (67226-2045-1) > 100 mL in 1 TUBE |
| Product NDC | 67226-2045 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110325 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Vivier Pharma, Inc. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 7.5; 7.5; 4.8 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |