AMBI FadeNormal Skin (Valeant Pharmaceuticals North America LLC)
Welcome to the PulseAid listing for the AMBI Fade drug offered from Valeant Pharmaceuticals North America 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: | Valeant Pharmaceuticals North America 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: | 2014-02-04 |
END MARKETING DATE: | 0000-00-00 |
AMBI Fade Normal Skin HUMAN OTC DRUG Details:
Item Description | AMBI Fade Normal Skin from Valeant Pharmaceuticals North America LLC |
LABELER NAME: | Valeant Pharmaceuticals North America LLC |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 20; 20(mg/g; mg/g) |
START MARKETING DATE: | 2014-02-04 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0187-5479_2e335de0-1593-4abe-94f0-26b492c83fb6 |
PRODUCT NDC: | 0187-5479 |
APPLICATION NUMBER: | part358A |
Other HYDROQUINONE; OCTINOXATE Pharmaceutical Manufacturers / Labelers: