Ulta BeautyBroad Spectrum SPF 30 Sunscreen (Prime Enterprises Inc.)


Welcome to the PulseAid listing for the Ulta Beauty 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: Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone
SUBSTANCE NAME: OCTISALATE; OXYBENZONE; OCTOCRYLENE; AVOBENZONE; HOMOSALATE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LOTION
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2016-12-27
END MARKETING DATE: 0000-00-00


Ulta Beauty Broad Spectrum SPF 30 Sunscreen HUMAN OTC DRUG Details:

Item DescriptionUlta Beauty Broad Spectrum SPF 30 Sunscreen from Prime Enterprises Inc.
LABELER NAME: Prime Enterprises Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 50.5; 20.2; 27.78; 30.3; 75.75(mg/mL; mg/mL; mg/mL; mg/mL; mg/mL)
START MARKETING DATE: 2016-12-27
END MARKETING DATE: 0000-00-00
PRODUCT ID: 58443-0244_44aa37e6-e697-022a-e054-00144ff88e88
PRODUCT NDC: 58443-0244
APPLICATION NUMBER: part352

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

Manufacturer / LabelerProprietary Name
Edgewell Personal Care Brands LLCBanana Boat
Prime Enterprises Inc.Ulta Beauty