Solar Moisturizer SPF 30 (Allure Labs, Inc.)


Welcome to the PulseAid listing for the Solar Moisturizer SPF 30 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: Octinoxate, Oxybenzone, Octisalate, Avobenzone, Octocrylene
SUBSTANCE NAME: OCTINOXATE; OXYBENZONE; OCTISALATE; AVOBENZONE; OCTOCRYLENE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2015-05-12
END MARKETING DATE: 0000-00-00


Solar Moisturizer SPF 30 HUMAN OTC DRUG Details:

Item DescriptionSolar Moisturizer SPF 30 from Allure Labs, Inc.
LABELER NAME: Allure Labs, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 7.5; 6; 5; 2; 1.5(mg/g; mg/g; mg/g; mg/g; mg/g)
START MARKETING DATE: 2015-05-12
END MARKETING DATE: 0000-00-00
PRODUCT ID: 62742-4078_f003ccad-e829-4783-a5c2-c78b5791c00e
PRODUCT NDC: 62742-4078
APPLICATION NUMBER: part352

Other OCTINOXATE; OXYBENZONE; OCTISALATE; AVOBENZONE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Allure Labs, IncDerma Brilliance Sunscreen SPF 30
Allure Labs, Inc.Solar Moisturizer SPF 30