Ulta BeautySPF 30 Broad Spectrum Sunscreen (Prime Packaging Inc.)


Welcome to the PulseAid listing for the Ulta Beauty drug offered from Prime Packaging 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 Packaging Inc.
NON-PROPRIETARY NAME: Avobenzone, Homosalate, Octisalate, Octocrylene and, Oxybenzone
SUBSTANCE NAME: AVOBENZONE; OCTISALATE; OCTOCRYLENE; OXYBENZONE; HOMOSALATE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: SPRAY
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2016-12-30
END MARKETING DATE: 0000-00-00


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

Item DescriptionUlta Beauty SPF 30 Broad Spectrum Sunscreen from Prime Packaging Inc.
LABELER NAME: Prime Packaging Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 25.2; 42; 23.1; 16.8; 63(mg/mL; mg/mL; mg/mL; mg/mL; mg/mL)
START MARKETING DATE: 2016-12-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 13630-0119_48ad466c-d899-3dd8-e054-00144ff8d46c
PRODUCT NDC: 13630-0119
APPLICATION NUMBER: part352

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

Manufacturer / LabelerProprietary Name
Bayer HealthCare LLC.Coppertone Defend and Care
Edgewell Personal Care Brands LLCBanana Boat
Prime Packaging Inc.Ulta Beauty