UltaBroad Spectrum SUNSCREEN SPF80 (Prime Enterprises, Inc.)


Welcome to the PulseAid listing for the Ulta drug offered from Prime Enterprises, 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: Prime Enterprises, Inc.
NON-PROPRIETARY NAME: Avobezone, Enzulizole, Homosalate, Octisalate, Octocrylene, and Oxybenzone
SUBSTANCE NAME: AVOBENZONE; ENSULIZOLE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LOTION
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2008-12-01
END MARKETING DATE: 0000-00-00


Ulta Broad Spectrum SUNSCREEN SPF80 HUMAN OTC DRUG Details:

Item DescriptionUlta Broad Spectrum SUNSCREEN SPF80 from Prime Enterprises, Inc.
LABELER NAME: Prime Enterprises, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 28.2; 9.4; 141; 47; 25.85; 37.6(mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL)
START MARKETING DATE: 2008-12-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 58443-0130_6d45ee32-b4eb-4e53-92f0-f5d874b1dc62
PRODUCT NDC: 58443-0130
APPLICATION NUMBER: part352

Other AVOBENZONE; ENSULIZOLE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Prime Enterprises, Inc.Ulta