PROVENCE CALENDULA AQUA SUN (NATURE REPUBLIC CO., LTD.)


Welcome to the PulseAid listing for the PROVENCE CALENDULA AQUA SUN drug offered from NATURE REPUBLIC 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: NATURE REPUBLIC CO., LTD.
NON-PROPRIETARY NAME: OCTINOXATE, OCTISALATE, HOMOSALATE
SUBSTANCE NAME: OCTINOXATE; OCTISALATE; HOMOSALATE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: GEL
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2015-02-01
END MARKETING DATE: 0000-00-00


PROVENCE CALENDULA AQUA SUN HUMAN OTC DRUG Details:

Item DescriptionPROVENCE CALENDULA AQUA SUN from NATURE REPUBLIC CO., LTD.
LABELER NAME: NATURE REPUBLIC CO., LTD.
DEA SCHEDULE:
ACTIVE STRENGTH: 3.25; 2.2; 2.2(mg/50mL; mg/50mL; mg/50mL)
START MARKETING DATE: 2015-02-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 51346-283_c733994b-4e3f-4883-a1ea-9b128d44bf6e
PRODUCT NDC: 51346-283
APPLICATION NUMBER: part352

Other OCTINOXATE; OCTISALATE; HOMOSALATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
21st Century Formulationsskin MD Natural
Gloves in a Bottle, IncGloves in a Bottle with SPF15
NATURE REPUBLIC CO., LTD.PROVENCE CALENDULA AQUA SUN