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 |