| Product NDC: | 43419-703 |
| Proprietary Name: | LANEIGE LIP TREATMENT |
| Non Proprietary Name: | OCTINOXATE |
| Active Ingredient(s): | .12 g/4g & nbsp; OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STICK |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43419-703 |
| Labeler Name: | AMOREPACIFIC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110901 |
| Package NDC: | 43419-703-07 |
| Package Description: | 4 g in 1 CYLINDER (43419-703-07) |
| NDC Code | 43419-703-07 |
| Proprietary Name | LANEIGE LIP TREATMENT |
| Package Description | 4 g in 1 CYLINDER (43419-703-07) |
| Product NDC | 43419-703 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE |
| Dosage Form Name | STICK |
| Route Name | TOPICAL |
| Start Marketing Date | 20110901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | AMOREPACIFIC |
| Substance Name | OCTINOXATE |
| Strength Number | .12 |
| Strength Unit | g/4g |
| Pharmaceutical Classes |