SUN Solar Defense Hydrating (Allure Labs, Inc.)
Welcome to the PulseAid listing for the SUN Solar Defense Hydrating drug offered from Allure Labs, 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: | Allure Labs, Inc. |
NON-PROPRIETARY NAME: | Zinc Oxide, Ethylhexyl Methoxycinnamate, Benzophenone, Ethylhexyl Salicylate |
SUBSTANCE NAME: | ZINC OXIDE; OCTINOXATE; OXYBENZONE; OCTISALATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | CREAM |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2010-01-01 |
END MARKETING DATE: | 0000-00-00 |
SUN Solar Defense Hydrating HUMAN OTC DRUG Details:
Item Description | SUN Solar Defense Hydrating from Allure Labs, Inc. |
LABELER NAME: | Allure Labs, Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 50; 75; 30; 50(mg/mL; mg/mL; mg/mL; mg/mL) |
START MARKETING DATE: | 2010-01-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62742-4037_cea5b90c-cb67-4803-910e-625cba66ff37 |
PRODUCT NDC: | 62742-4037 |
APPLICATION NUMBER: | part352 |
Other ZINC OXIDE; OCTINOXATE; OXYBENZONE; OCTISALATE Pharmaceutical Manufacturers / Labelers: