MY SUNNY WATERY SUN ESSENCE (TONYMOLY CO.,LTD)
Welcome to the PulseAid listing for the MY SUNNY WATERY SUN ESSENCE drug offered from TONYMOLY 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: | TONYMOLY CO.,LTD |
NON-PROPRIETARY NAME: | OCTINOXATE, HOMOSALATE, OCTISALATE, OCTOCRYLENE |
SUBSTANCE NAME: | OCTINOXATE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | TOPICAL |
DOSAGE FORM: | CREAM |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2017-06-01 |
END MARKETING DATE: | 0000-00-00 |
MY SUNNY WATERY SUN ESSENCE HUMAN OTC DRUG Details:
Item Description | MY SUNNY WATERY SUN ESSENCE from TONYMOLY CO.,LTD |
LABELER NAME: | TONYMOLY CO.,LTD |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 3.4; 3; 2.25; 1.25(g/50mL; g/50mL; g/50mL; g/50mL) |
START MARKETING DATE: | 2017-06-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 59078-324_a07fd3b0-c984-49f4-b627-42fb14b67b41 |
PRODUCT NDC: | 59078-324 |
APPLICATION NUMBER: | part352 |
Other OCTINOXATE; HOMOSALATE; OCTISALATE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers: