| 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 |