Derma Soleil Dry Sport SPF 30 (Derma Soleil)
Welcome to the PulseAid listing for the Derma Soleil Dry Sport SPF 30 drug offered from Derma Soleil. 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: | Derma Soleil |
NON-PROPRIETARY NAME: | Octocrylene, Octyl Methoxycinnamate, Octyl Salicylate, Oxybenzone |
SUBSTANCE NAME: | OCTINOXATE; OCTISALATE; OXYBENZONE; OCTOCRYLENE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | LOTION |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2017-07-20 |
END MARKETING DATE: | 0000-00-00 |
Derma Soleil Dry Sport SPF 30 HUMAN OTC DRUG Details:
Item Description | Derma Soleil Dry Sport SPF 30 from Derma Soleil |
LABELER NAME: | Derma Soleil |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 7.5; 4; 5; 4(g/100mL; g/100mL; g/100mL; g/100mL) |
START MARKETING DATE: | 2017-07-20 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 69711-308_55135e2c-52e9-3e36-e054-00144ff8d46c |
PRODUCT NDC: | 69711-308 |
APPLICATION NUMBER: | part352 |
Other OCTINOXATE; OCTISALATE; OXYBENZONE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers: