AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID (AMARTEINTERNATIONAL CO., LTD.)
Welcome to the PulseAid listing for the AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID drug offered from AMARTEINTERNATIONAL 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: | AMARTEINTERNATIONAL CO., LTD. |
| NON-PROPRIETARY NAME: | Octinoxate, Titanium Dioxide, Octisalate, Zinc Oxide |
| SUBSTANCE NAME: | OCTINOXATE; TITANIUM DIOXIDE; OCTISALATE; ZINC OXIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | CREAM |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2014-10-01 |
| END MARKETING DATE: | 0000-00-00 |
AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID HUMAN OTC DRUG Details:
| Item Description | AMARTE ULTRA VEIL ULTRA LIGHT SUNSCREEN FLUID from AMARTEINTERNATIONAL CO., LTD. |
| LABELER NAME: | AMARTEINTERNATIONAL CO., LTD. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 4.9; 3.78; 3.5; 2.1(mg/70mL; mg/70mL; mg/70mL; mg/70mL) |
| START MARKETING DATE: | 2014-10-01 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 69352-020_e4aa261a-6314-4e03-8803-b3a1879d4969 |
| PRODUCT NDC: | 69352-020 |
| APPLICATION NUMBER: | part352 |
Other OCTINOXATE; TITANIUM DIOXIDE; OCTISALATE; ZINC OXIDE Pharmaceutical Manufacturers / Labelers:
