| Product NDC: | 43419-811 |
| Proprietary Name: | Laneige |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | 4.9; 4.067; 1.372 mL/70mL; mL/70mL; mL/70mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43419-811 |
| Labeler Name: | AMOREPACIFIC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100601 |
| Package NDC: | 43419-811-83 |
| Package Description: | 70 mL in 1 TUBE (43419-811-83) |
| NDC Code | 43419-811-83 |
| Proprietary Name | Laneige |
| Package Description | 70 mL in 1 TUBE (43419-811-83) |
| Product NDC | 43419-811 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | AMOREPACIFIC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 4.9; 4.067; 1.372 |
| Strength Unit | mL/70mL; mL/70mL; mL/70mL |
| Pharmaceutical Classes |