PREMIUM ULTRA UV PURE SUN (Purecell Korea Co., Ltd.)


Welcome to the PulseAid listing for the PREMIUM ULTRA UV PURE SUN drug offered from Purecell Korea Co., Ltd.. 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: Purecell Korea Co., Ltd.
NON-PROPRIETARY NAME: Octocrylene, Ethylhexyl Methoxycinnamate, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Ethylhexyl Salicylate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine
SUBSTANCE NAME: OCTINOXATE; DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE; OCTISALATE; BEMOTRIZINOL; OCTOCRYLENE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: STICK
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2017-06-01
END MARKETING DATE: 0000-00-00


PREMIUM ULTRA UV PURE SUN HUMAN OTC DRUG Details:

Item DescriptionPREMIUM ULTRA UV PURE SUN from Purecell Korea Co., Ltd.
LABELER NAME: Purecell Korea Co., Ltd.
DEA SCHEDULE:
ACTIVE STRENGTH: 7; 7; 5; 2; 8(g/100g; g/100g; g/100g; g/100g; g/100g)
START MARKETING DATE: 2017-06-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 71609-0009_56375b26-8b45-74c8-e054-00144ff88e88
PRODUCT NDC: 71609-0009
APPLICATION NUMBER: part352

Other OCTINOXATE; DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE; OCTISALATE; BEMOTRIZINOL; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Purecell Korea Co., Ltd.PREMIUM ULTRA UV PURE SUN