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Laneige Skin Veil
Laneige Skin Veil - 43419-853-08 - (OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE)
Drug Information of Laneige Skin Veil
| Product NDC: | 43419-853 |
| Proprietary Name: | Laneige Skin Veil |
| Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | .05; .0955; .012 mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Laneige Skin Veil
| Product NDC: | 43419-853 |
| Labeler Name: | AMOREPACIFIC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100915 |
Package Information of Laneige Skin Veil
| Package NDC: | 43419-853-08 |
| Package Description: | 1 BOTTLE in 1 CARTON (43419-853-08) > 30 mL in 1 BOTTLE |
NDC Information of Laneige Skin Veil
| NDC Code | 43419-853-08 |
| Proprietary Name | Laneige Skin Veil |
| Package Description | 1 BOTTLE in 1 CARTON (43419-853-08) > 30 mL in 1 BOTTLE |
| Product NDC | 43419-853 |
| 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 | 20100915 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | AMOREPACIFIC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .05; .0955; .012 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
