TONYMOLY My Sunny All SunSpray (Tonymoly Co., Ltd.)
Welcome to the PulseAid listing for the TONYMOLY My Sunny All SunSpray 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: | Ethylhexyl Methoxycinnamate |
| SUBSTANCE NAME: | TITANIUM DIOXIDE; OCTOCRYLENE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | SPRAY |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2016-01-14 |
| END MARKETING DATE: | 0000-00-00 |
TONYMOLY My Sunny All SunSpray HUMAN OTC DRUG Details:
| Item Description | TONYMOLY My Sunny All SunSpray from Tonymoly Co., Ltd. |
| LABELER NAME: | Tonymoly Co., Ltd. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 20557.8; 4725(mg/150mL; mg/150mL) |
| START MARKETING DATE: | 2016-01-14 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 59078-120_2af68f0b-4b4d-5387-e054-00144ff8d46c |
| PRODUCT NDC: | 59078-120 |
| APPLICATION NUMBER: | part352 |
Other TITANIUM DIOXIDE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers:
