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 DescriptionSUN 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:

Manufacturer / LabelerProprietary Name
Allure Labs, Inc.SUN Solar Defense Hydrating