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 |