Sunspray (Kiss My Face, LLC)


Welcome to the PulseAid listing for the Sunspray drug offered from Kiss My Face, LLC. 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: Kiss My Face, LLC
NON-PROPRIETARY NAME: Avobenzone, Homosalate, Octinoxate, Octisalate, Titanium Dioxide
SUBSTANCE NAME: AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: SPRAY
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2015-01-01
END MARKETING DATE: 0000-00-00


Sunspray HUMAN OTC DRUG Details:

Item DescriptionSunspray from Kiss My Face, LLC
LABELER NAME: Kiss My Face, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 5; 7.5; 6.5; 2(g/100g; g/100g; g/100g; g/100g; g/100g)
START MARKETING DATE: 2015-01-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 65364-218_c9c86d45-0999-4b7d-81c1-9605fec5192d
PRODUCT NDC: 65364-218
APPLICATION NUMBER: part352

Other AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Kiss My Face, LLCSunspray