| Product NDC: | 58414-2046 |
| Proprietary Name: | Exuviance Essential Daily Defense SPF 30 |
| Non Proprietary Name: | OCTINOXATE and TITANIUM DIOXIDE |
| Active Ingredient(s): | 60; 40 mg/g; mg/g & nbsp; OCTINOXATE and TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58414-2046 |
| Labeler Name: | NeoStrata Company Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130710 |
| Package NDC: | 58414-2046-1 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (58414-2046-1) > 50 g in 1 BOTTLE, PUMP |
| NDC Code | 58414-2046-1 |
| Proprietary Name | Exuviance Essential Daily Defense SPF 30 |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (58414-2046-1) > 50 g in 1 BOTTLE, PUMP |
| Product NDC | 58414-2046 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE and TITANIUM DIOXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130710 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | NeoStrata Company Inc. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 60; 40 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |