| Product NDC: | 63505-006 |
| Proprietary Name: | YVES ROCHER hydra vegetal HYDRATING DAY SPF 25 SUNSCREEN |
| Non Proprietary Name: | ENSULIZOLE, OCTINOXATE, OCTISALATE, ZINC OXIDE |
| Active Ingredient(s): | 40; 75; 50; 49 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; ENSULIZOLE, OCTINOXATE, OCTISALATE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63505-006 |
| Labeler Name: | Yves Rocher North America Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130605 |
| Package NDC: | 63505-006-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (63505-006-01) > 50 mL in 1 BOTTLE |
| NDC Code | 63505-006-01 |
| Proprietary Name | YVES ROCHER hydra vegetal HYDRATING DAY SPF 25 SUNSCREEN |
| Package Description | 1 BOTTLE in 1 CARTON (63505-006-01) > 50 mL in 1 BOTTLE |
| Product NDC | 63505-006 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ENSULIZOLE, OCTINOXATE, OCTISALATE, ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130605 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Yves Rocher North America Inc |
| Substance Name | ENSULIZOLE; OCTINOXATE; OCTISALATE; ZINC OXIDE |
| Strength Number | 40; 75; 50; 49 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |