| Product NDC: | 76485-1031 |
| Proprietary Name: | Match Perfection SPF 18 |
| Non Proprietary Name: | Octinoxate Titanium Dioxide |
| Active Ingredient(s): | 1.2; 1.5 mL/30mL; mL/30mL & nbsp; Octinoxate Titanium Dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76485-1031 |
| Labeler Name: | Rimmel Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120915 |
| Package NDC: | 76485-1031-1 |
| Package Description: | 30 mL in 1 BOTTLE, DISPENSING (76485-1031-1) |
| NDC Code | 76485-1031-1 |
| Proprietary Name | Match Perfection SPF 18 |
| Package Description | 30 mL in 1 BOTTLE, DISPENSING (76485-1031-1) |
| Product NDC | 76485-1031 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate Titanium Dioxide |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120915 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Rimmel Inc. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 1.2; 1.5 |
| Strength Unit | mL/30mL; mL/30mL |
| Pharmaceutical Classes |