Moroccanoil Sun Oil (Moroccanoil, Inc.)


Welcome to the PulseAid listing for the Moroccanoil Sun Oil drug offered from Moroccanoil, 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: Moroccanoil, Inc.
NON-PROPRIETARY NAME: Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
SUBSTANCE NAME: HOMOSALATE; OCTISALATE; OXYBENZONE; OCTOCRYLENE; AVOBENZONE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LOTION
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2015-06-01
END MARKETING DATE: 0000-00-00


Moroccanoil Sun Oil HUMAN OTC DRUG Details:

Item DescriptionMoroccanoil Sun Oil from Moroccanoil, Inc.
LABELER NAME: Moroccanoil, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 12; 5; 6; 2.5; 3(g/100mL; g/100mL; g/100mL; g/100mL; g/100mL)
START MARKETING DATE: 2015-06-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 69942-030_56696421-fa94-5107-e054-00144ff8d46c
PRODUCT NDC: 69942-030
APPLICATION NUMBER: part352

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

Manufacturer / LabelerProprietary Name
Moroccanoil, Inc.Moroccanoil Sun Oil
Sun & Skin Care Research, IncOcean Potion Quick Dry SPF 70 Sunscreen
Sun & Skin Care Research, LLCNO-AD 85 Sunscreen