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 Description | Moroccanoil Sun Oil from Moroccanoil, Inc. |
LABELER NAME: | Moroccanoil, Inc. |
DEA SCHEDULE: |
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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: