| Product NDC: | 59351-0320 |
| Proprietary Name: | Rimmel London |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE |
| Active Ingredient(s): | 1.2; .9 mL/30mL; mL/30mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59351-0320 |
| Labeler Name: | Lancaster S.A.M. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101006 |
| Package NDC: | 59351-0320-1 |
| Package Description: | 30 mL in 1 BOTTLE, DISPENSING (59351-0320-1) |
| NDC Code | 59351-0320-1 |
| Proprietary Name | Rimmel London |
| Package Description | 30 mL in 1 BOTTLE, DISPENSING (59351-0320-1) |
| Product NDC | 59351-0320 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20101006 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Lancaster S.A.M. |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
| Strength Number | 1.2; .9 |
| Strength Unit | mL/30mL; mL/30mL |
| Pharmaceutical Classes |