Laneige - 43419-811-83 - (OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE)

Alphabetical Index


Drug Information of Laneige

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)

Labeler Information of Laneige

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 Information of Laneige

Package NDC: 43419-811-83
Package Description: 70 mL in 1 TUBE (43419-811-83)

NDC Information of Laneige

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

Complete Information of Laneige


General Information