Product NDC: | 66171-123 |
Proprietary Name: | Dr.Denese SPF 30 Defense Day |
Non Proprietary Name: | ZINC OXIDE, OCTINOXATE |
Active Ingredient(s): | 7.5; 7.5 g/100g; g/100g & nbsp; ZINC OXIDE, OCTINOXATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66171-123 |
Labeler Name: | SkinScience Labs, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110521 |
Package NDC: | 66171-123-02 |
Package Description: | 45 g in 1 TUBE (66171-123-02) |
NDC Code | 66171-123-02 |
Proprietary Name | Dr.Denese SPF 30 Defense Day |
Package Description | 45 g in 1 TUBE (66171-123-02) |
Product NDC | 66171-123 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ZINC OXIDE, OCTINOXATE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110521 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | SkinScience Labs, Inc |
Substance Name | OCTINOXATE; ZINC OXIDE |
Strength Number | 7.5; 7.5 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |