| Product NDC: | 59351-0333 |
| Proprietary Name: | Rimmel London |
| Non Proprietary Name: | Octinoxate, Octisalate |
| Active Ingredient(s): | .012; .12 mL/6mL; mL/6mL & nbsp; Octinoxate, Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59351-0333 |
| Labeler Name: | Lancaster S.A.M. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101020 |
| Package NDC: | 59351-0333-1 |
| Package Description: | 6 mL in 1 TUBE (59351-0333-1) |
| NDC Code | 59351-0333-1 |
| Proprietary Name | Rimmel London |
| Package Description | 6 mL in 1 TUBE (59351-0333-1) |
| Product NDC | 59351-0333 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101020 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Lancaster S.A.M. |
| Substance Name | OCTINOXATE; OCTISALATE |
| Strength Number | .012; .12 |
| Strength Unit | mL/6mL; mL/6mL |
| Pharmaceutical Classes |