Derma Soleil Natural Sunblock SPF 15 (Derma Soleil)


Welcome to the PulseAid listing for the Derma Soleil Natural Sunblock SPF 15 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: OCTISALATE; OXYBENZONE; OCTINOXATE; 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 Natural Sunblock SPF 15 HUMAN OTC DRUG Details:

Item DescriptionDerma Soleil Natural Sunblock SPF 15 from Derma Soleil
LABELER NAME: Derma Soleil
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 4; 6; 3(g/100mL; g/100mL; g/100mL; g/100mL)
START MARKETING DATE: 2017-07-20
END MARKETING DATE: 0000-00-00
PRODUCT ID: 69711-152_5514545e-34df-4500-e054-00144ff88e88
PRODUCT NDC: 69711-152
APPLICATION NUMBER: part352

Other OCTISALATE; OXYBENZONE; OCTINOXATE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Derma SoleilDerma Soleil Natural Sunblock SPF 15