SkinTx UV Pro Broad Spectrum SPF30 (Dermolab Pharma Ltd)
Welcome to the PulseAid listing for the SkinTx UV Pro Broad Spectrum SPF30 drug offered from Dermolab Pharma Ltd. 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: | Dermolab Pharma Ltd |
NON-PROPRIETARY NAME: | ZINC OXIDE, OCTINOXATE, OCTISALATE |
SUBSTANCE NAME: | ZINC OXIDE; OCTINOXATE; OCTISALATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2015-05-14 |
END MARKETING DATE: | 0000-00-00 |
SkinTx UV Pro Broad Spectrum SPF30 HUMAN OTC DRUG Details:
Item Description | SkinTx UV Pro Broad Spectrum SPF30 from Dermolab Pharma Ltd |
LABELER NAME: | Dermolab Pharma Ltd |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 99; 75; 50(mg/mL; mg/mL; mg/mL) |
START MARKETING DATE: | 2015-05-14 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 42521-2930_20265376-77ff-42b9-9a76-d8914a12d342 |
PRODUCT NDC: | 42521-2930 |
APPLICATION NUMBER: | part352 |
Other ZINC OXIDE; OCTINOXATE; OCTISALATE Pharmaceutical Manufacturers / Labelers: