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Laneige Skin Veil - 43419-856-09 - (OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE)

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Drug Information of Laneige Skin Veil

Product NDC: 43419-856
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: 43419-856
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: 43419-856-09
Package Description: 1 BOTTLE in 1 CARTON (43419-856-09) > 30 mL in 1 BOTTLE

NDC Information of Laneige Skin Veil

NDC Code 43419-856-09
Proprietary Name Laneige Skin Veil
Package Description 1 BOTTLE in 1 CARTON (43419-856-09) > 30 mL in 1 BOTTLE
Product NDC 43419-856
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

Complete Information of Laneige Skin Veil


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