| Product NDC: | 62802-600 |
| Proprietary Name: | OP Dark Formula Xtreme Tanning 4 |
| Non Proprietary Name: | octinoxate, octisalate |
| Active Ingredient(s): | 3; 2 mL/100mL; mL/100mL & nbsp; octinoxate, octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62802-600 |
| Labeler Name: | Sun & Skin Care Research, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120101 |
| Package NDC: | 62802-600-08 |
| Package Description: | 251 mL in 1 BOTTLE (62802-600-08) |
| NDC Code | 62802-600-08 |
| Proprietary Name | OP Dark Formula Xtreme Tanning 4 |
| Package Description | 251 mL in 1 BOTTLE (62802-600-08) |
| Product NDC | 62802-600 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, octisalate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Sun & Skin Care Research, LLC |
| Substance Name | OCTINOXATE; OCTISALATE |
| Strength Number | 3; 2 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |