Home > National Drug Code (NDC) > Sulwhasoo Lumitouch

Sulwhasoo Lumitouch - 43419-719-30 - (OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE)

Alphabetical Index


Drug Information of Sulwhasoo Lumitouch

Product NDC: 43419-719
Proprietary Name: Sulwhasoo Lumitouch
Non Proprietary Name: OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE
Active Ingredient(s): .352; 1.533; .216    g/11g; g/11g; g/11g & nbsp;   OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Sulwhasoo Lumitouch

Product NDC: 43419-719
Labeler Name: AMOREPACIFIC CO.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100901

Package Information of Sulwhasoo Lumitouch

Package NDC: 43419-719-30
Package Description: 11 g in 1 JAR (43419-719-30)

NDC Information of Sulwhasoo Lumitouch

NDC Code 43419-719-30
Proprietary Name Sulwhasoo Lumitouch
Package Description 11 g in 1 JAR (43419-719-30)
Product NDC 43419-719
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100901
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name AMOREPACIFIC CO.
Substance Name OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number .352; 1.533; .216
Strength Unit g/11g; g/11g; g/11g
Pharmaceutical Classes

Complete Information of Sulwhasoo Lumitouch


General Information