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 Description | Porcelana 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: