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LANEIGE SNOW CRYSTAL - 43419-858-22 - (Octinoxate, TITANIUM DIOXIDE, and ZINC OXIDE)

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Drug Information of LANEIGE SNOW CRYSTAL

Product NDC: 43419-858
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: 43419-858
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: 43419-858-22
Package Description: 1 BOTTLE in 1 CARTON (43419-858-22) > 30 mL in 1 BOTTLE

NDC Information of LANEIGE SNOW CRYSTAL

NDC Code 43419-858-22
Proprietary Name LANEIGE SNOW CRYSTAL
Package Description 1 BOTTLE in 1 CARTON (43419-858-22) > 30 mL in 1 BOTTLE
Product NDC 43419-858
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

Complete Information of LANEIGE SNOW CRYSTAL


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