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LANEIGE SNOW CRYSTAL
LANEIGE SNOW CRYSTAL - 43419-857-21 - (Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE)
Drug Information of LANEIGE SNOW CRYSTAL
| Product NDC: | 43419-857 |
| Proprietary Name: | LANEIGE SNOW CRYSTAL |
| Non Proprietary Name: | Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | .05; .0582; .0098 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 SNOW CRYSTAL
| Product NDC: | 43419-857 |
| 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 SNOW CRYSTAL
| Package NDC: | 43419-857-21 |
| Package Description: | 1 BOTTLE in 1 CARTON (43419-857-21) > 30 mL in 1 BOTTLE |
NDC Information of LANEIGE SNOW CRYSTAL
| NDC Code | 43419-857-21 |
| Proprietary Name | LANEIGE SNOW CRYSTAL |
| Package Description | 1 BOTTLE in 1 CARTON (43419-857-21) > 30 mL in 1 BOTTLE |
| Product NDC | 43419-857 |
| 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; .0582; .0098 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
