Porcelana Day Skin Lightening (Ultimark Products LLC)


Welcome to the PulseAid listing for the Porcelana Day Skin Lightening drug offered from Ultimark Products LLC. 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: Ultimark Products LLC
NON-PROPRIETARY NAME: Hydroquinone and Octinoxate
SUBSTANCE NAME: HYDROQUINONE; OCTINOXATE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2011-04-01
END MARKETING DATE: 0000-00-00


Porcelana Day Skin Lightening HUMAN OTC DRUG Details:

Item DescriptionPorcelana Day Skin Lightening from Ultimark Products LLC
LABELER NAME: Ultimark Products LLC
DEA SCHEDULE:
ACTIVE STRENGTH: .02; .025(g/g; g/g)
START MARKETING DATE: 2011-04-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 51545-110_ff9f71bb-a9ed-40f7-9c83-3f95f94addb1
PRODUCT NDC: 51545-110
APPLICATION NUMBER: part358A

Other HYDROQUINONE; OCTINOXATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Bluefield Associates, Inc.Medicated Fade Creme with Sunscreen
International Beauty ExchangeTopiclear Skin Lightening
Ultimark Products LLCPorcelana Day Skin Lightening
Valeant Pharmaceuticals North America LLCAMBI Fade