CLEMATIS Morning Dew CC (Coshub Co., Ltd.)


Welcome to the PulseAid listing for the CLEMATIS Morning Dew CC drug offered from Coshub 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: Coshub Co., Ltd.
NON-PROPRIETARY NAME: Octinoxate, Titanium Dioxide, Octisalate, Homosalate
SUBSTANCE NAME: OCTINOXATE; TITANIUM DIOXIDE; OCTISALATE; HOMOSALATE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2017-08-01
END MARKETING DATE: 0000-00-00


CLEMATIS Morning Dew CC HUMAN OTC DRUG Details:

Item DescriptionCLEMATIS Morning Dew CC from Coshub Co., Ltd.
LABELER NAME: Coshub Co., Ltd.
DEA SCHEDULE:
ACTIVE STRENGTH: 3.5; 1.69; 1.5; 1.5(g/50mL; g/50mL; g/50mL; g/50mL)
START MARKETING DATE: 2017-08-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 71702-110_9d2c27ed-d394-4764-86fd-a3d2293a68e8
PRODUCT NDC: 71702-110
APPLICATION NUMBER: part352

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

Manufacturer / LabelerProprietary Name
Coshub Co., Ltd.CLEMATIS Morning Dew CC