SHISEIDO WHITE LUCENT (SHISEIDO AMERICA INC.)


Welcome to the PulseAid listing for the SHISEIDO WHITE LUCENT drug offered from SHISEIDO AMERICA 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: SHISEIDO AMERICA INC.
NON-PROPRIETARY NAME: Ensulizole, Octinoxate, and Titanium Dioxide
SUBSTANCE NAME: ENSULIZOLE; OCTINOXATE; TITANIUM DIOXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2010-02-01
END MARKETING DATE: 0000-00-00


SHISEIDO WHITE LUCENT HUMAN OTC DRUG Details:

Item DescriptionSHISEIDO WHITE LUCENT from SHISEIDO AMERICA INC.
LABELER NAME: SHISEIDO AMERICA INC.
DEA SCHEDULE:
ACTIVE STRENGTH: 1.275; 3.774; .969(g/51g; g/51g; g/51g)
START MARKETING DATE: 2010-02-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 52686-227_1e4b266f-4f72-494f-a186-fa748cd1ea91
PRODUCT NDC: 52686-227
APPLICATION NUMBER: part352

Other ENSULIZOLE; OCTINOXATE; TITANIUM DIOXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
SHISEIDO AMERICA INC.SHISEIDO WHITE LUCENT
SHISEIDO AMERICAS CORPORATIONCLE DE PEAU BEAUTE CORRECTING VEIL