Product NDC: | 53208-518 |
Proprietary Name: | OHUI SUNSCIENCE LUMINOUS WHITENING SUNBLOCK |
Non Proprietary Name: | ENSULIZOLE, OCTISALATE, BEMOTRIZINOL, OCTOCRYLENE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, ZINC OXIDE, TITANIUM DIOXIDE, ATRACTYLODES JAPONICA ROOT OIL |
Active Ingredient(s): | .525; 1.5; 1; 3.9; 4.7; 5; 3.67; 12.3 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; ENSULIZOLE, OCTISALATE, BEMOTRIZINOL, OCTOCRYLENE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, ZINC OXIDE, TITANIUM DIOXIDE, ATRACTYLODES JAPONICA ROOT OIL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53208-518 |
Labeler Name: | LG Household and Healthcare, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110406 |
Package NDC: | 53208-518-02 |
Package Description: | 1 CONTAINER in 1 BOX (53208-518-02) > 50 mL in 1 CONTAINER (53208-518-01) |
NDC Code | 53208-518-02 |
Proprietary Name | OHUI SUNSCIENCE LUMINOUS WHITENING SUNBLOCK |
Package Description | 1 CONTAINER in 1 BOX (53208-518-02) > 50 mL in 1 CONTAINER (53208-518-01) |
Product NDC | 53208-518 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ENSULIZOLE, OCTISALATE, BEMOTRIZINOL, OCTOCRYLENE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, ZINC OXIDE, TITANIUM DIOXIDE, ATRACTYLODES JAPONICA ROOT OIL |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110406 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | LG Household and Healthcare, Inc. |
Substance Name | ATRACTYLODES JAPONICA ROOT OIL; BEMOTRIZINOL; DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE; ENSULIZOLE; OCTISALATE; OCTOCRYLENE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | .525; 1.5; 1; 3.9; 4.7; 5; 3.67; 12.3 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |