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LANEIGE SKIN VEIL
LANEIGE SKIN VEIL - 43419-852-00 - (Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE)
Drug Information of LANEIGE SKIN VEIL
| Product NDC: | 43419-852 |
| Proprietary Name: | LANEIGE SKIN VEIL |
| Non Proprietary Name: | Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | 1.5; 1.11; .36 mL/30mL; mL/30mL; mL/30mL & 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: | 43419-852 |
| Labeler Name: | AMOREPACIFIC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100901 |
Package Information of LANEIGE SKIN VEIL
| Package NDC: | 43419-852-00 |
| Package Description: | 30 mL in 1 BOTTLE (43419-852-00) |
NDC Information of LANEIGE SKIN VEIL
| NDC Code | 43419-852-00 |
| Proprietary Name | LANEIGE SKIN VEIL |
| Package Description | 30 mL in 1 BOTTLE (43419-852-00) |
| Product NDC | 43419-852 |
| 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 | 20100901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | AMOREPACIFIC |
| Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 1.5; 1.11; .36 |
| Strength Unit | mL/30mL; mL/30mL; mL/30mL |
| Pharmaceutical Classes |
