Ocean Potion Instant Dry 70 Mist Sunscreen (Sun & Skin Care Research, LLC)


Welcome to the PulseAid listing for the Ocean Potion Instant Dry 70 Mist Sunscreen drug offered from Sun & Skin Care Research, 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: Sun & Skin Care Research, LLC
NON-PROPRIETARY NAME: avobenzone, homosalate, octisalate, octocrylene, oxybenzone
SUBSTANCE NAME: HOMOSALATE; OCTISALATE; OCTOCRYLENE; AVOBENZONE; OXYBENZONE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: SPRAY
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2012-01-01
END MARKETING DATE: 0000-00-00


Ocean Potion Instant Dry 70 Mist Sunscreen HUMAN OTC DRUG Details:

Item DescriptionOcean Potion Instant Dry 70 Mist Sunscreen from Sun & Skin Care Research, LLC
LABELER NAME: Sun & Skin Care Research, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 15; 5; 2; 2; 6(g/100g; g/100g; g/100g; g/100g; g/100g)
START MARKETING DATE: 2012-01-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 62802-644_29b3b675-0296-4222-b43a-2f16752715c0
PRODUCT NDC: 62802-644
APPLICATION NUMBER: part352

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

Manufacturer / LabelerProprietary Name
Sun & Skin Care Research, LLCOcean Potion Instant Dry 70 Mist Sunscreen