Product NDC: | 43419-021 |
Proprietary Name: | Sulwhasoo Lumitouch Foundation |
Non Proprietary Name: | OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
Active Ingredient(s): | .9; .498; .588 mL/30mL; mL/30mL; mL/30mL & nbsp; OCTINOXATE, TITANIUM DIOXIDE, and ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43419-021 |
Labeler Name: | AMOREPACIFIC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110103 |
Package NDC: | 43419-021-04 |
Package Description: | 30 mL in 1 JAR (43419-021-04) |
NDC Code | 43419-021-04 |
Proprietary Name | Sulwhasoo Lumitouch Foundation |
Package Description | 30 mL in 1 JAR (43419-021-04) |
Product NDC | 43419-021 |
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 | 20110103 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | AMOREPACIFIC |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | .9; .498; .588 |
Strength Unit | mL/30mL; mL/30mL; mL/30mL |
Pharmaceutical Classes |