| Product NDC: | 68026-420 |
| Proprietary Name: | Cellular Luxe Lip Treatment SPF 15 |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE |
| Active Ingredient(s): | 6; 3 g/100g; g/100g & nbsp; OCTINOXATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIPSTICK |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68026-420 |
| Labeler Name: | La Prairie, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110411 |
| Package NDC: | 68026-420-35 |
| Package Description: | 1 BOTTLE in 1 PACKAGE (68026-420-35) > 3.5 g in 1 BOTTLE |
| NDC Code | 68026-420-35 |
| Proprietary Name | Cellular Luxe Lip Treatment SPF 15 |
| Package Description | 1 BOTTLE in 1 PACKAGE (68026-420-35) > 3.5 g in 1 BOTTLE |
| Product NDC | 68026-420 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE |
| Dosage Form Name | LIPSTICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20110411 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | La Prairie, Inc. |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 6; 3 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |