| Product NDC: | 61957-0601 |
| Proprietary Name: | DIORSNOW White Reveal UVB Protection Sunscreen Translucent SPF 50 |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE |
| Active Ingredient(s): | 7.49; 3.55; 19 mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 61957-0601 |
| Labeler Name: | Parfums Christian Dior |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120719 |
| Package NDC: | 61957-0601-1 |
| Package Description: | 40 mL in 1 BOTTLE (61957-0601-1) |
| NDC Code | 61957-0601-1 |
| Proprietary Name | DIORSNOW White Reveal UVB Protection Sunscreen Translucent SPF 50 |
| Package Description | 40 mL in 1 BOTTLE (61957-0601-1) |
| Product NDC | 61957-0601 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120719 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Parfums Christian Dior |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 7.49; 3.55; 19 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |