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 Description | PREMIUM ULTRA UV PURE SUN from Purecell Korea Co., Ltd. |
LABELER NAME: | Purecell Korea Co., Ltd. |
DEA SCHEDULE: |
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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: