OHUI SUNSCIENCE LUMINOUS WHITENING SUNBLOCK (LG Household and Healthcare, Inc.)


Welcome to the PulseAid listing for the OHUI SUNSCIENCE LUMINOUS WHITENING SUNBLOCK drug offered from LG Household and Healthcare, Inc.. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: LG Household and Healthcare, Inc.
NON-PROPRIETARY NAME: ENSULIZOLE, OCTISALATE, BEMOTRIZINOL, OCTOCRYLENE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, ZINC OXIDE, TITANIUM DIOXIDE, ATRACTYLODES JAPONICA ROOT OIL
SUBSTANCE NAME: ENSULIZOLE; OCTISALATE; BEMOTRIZINOL; OCTOCRYLENE; DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE; ZINC OXIDE; TITANIUM DIOXIDE; ATRACTYLODES JAPONICA ROOT OIL
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2011-04-06
END MARKETING DATE: 0000-00-00


OHUI SUNSCIENCE LUMINOUS WHITENING SUNBLOCK HUMAN OTC DRUG Details:

Item DescriptionOHUI SUNSCIENCE LUMINOUS WHITENING SUNBLOCK from LG Household and Healthcare, Inc.
LABELER NAME: LG Household and Healthcare, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 3.9; 4.7; 1.5; 5; 1; 12.3; 3.67; .525(mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL)
START MARKETING DATE: 2011-04-06
END MARKETING DATE: 0000-00-00
PRODUCT ID: 53208-518_2c7b1f69-5b49-44a9-90a8-0f3552e75c32
PRODUCT NDC: 53208-518
APPLICATION NUMBER: part352

Other ENSULIZOLE; OCTISALATE; BEMOTRIZINOL; OCTOCRYLENE; DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE; ZINC OXIDE; TITANIUM DIOXIDE; ATRACTYLODES JAPONICA ROOT OIL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
LG Household and Healthcare, Inc.OHUI SUNSCIENCE LUMINOUS WHITENING SUNBLOCK