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 |