Product NDC: | 51727-0631 |
Proprietary Name: | Urban Defense |
Non Proprietary Name: | Octocrylene and Octinoxate |
Active Ingredient(s): | 3.75; 4 mL/50mL; mL/50mL & nbsp; Octocrylene and Octinoxate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | EMULSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51727-0631 |
Labeler Name: | Urban Decay Cosmetics, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120716 |
Package NDC: | 51727-0631-1 |
Package Description: | 1 TUBE in 1 CARTON (51727-0631-1) > 50 mL in 1 TUBE |
NDC Code | 51727-0631-1 |
Proprietary Name | Urban Defense |
Package Description | 1 TUBE in 1 CARTON (51727-0631-1) > 50 mL in 1 TUBE |
Product NDC | 51727-0631 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octocrylene and Octinoxate |
Dosage Form Name | EMULSION |
Route Name | TOPICAL |
Start Marketing Date | 20120716 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Urban Decay Cosmetics, LLC |
Substance Name | OCTINOXATE; OCTOCRYLENE |
Strength Number | 3.75; 4 |
Strength Unit | mL/50mL; mL/50mL |
Pharmaceutical Classes |