| Product NDC: | 51727-0633 |
| 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: | 51727-0633 |
| 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: | 51727-0633-1 |
| Package Description: | 1 TUBE in 1 CARTON (51727-0633-1) > 50 mL in 1 TUBE |
| NDC Code | 51727-0633-1 |
| Proprietary Name | Urban Defense |
| Package Description | 1 TUBE in 1 CARTON (51727-0633-1) > 50 mL in 1 TUBE |
| Product NDC | 51727-0633 |
| 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 |