Dr.Jart Every Sun Day Sunscreen SPF 50 (Have & Be Co., Ltd.)
Welcome to the PulseAid listing for the Dr.Jart Every Sun Day Sunscreen SPF 50 drug offered from Have & Be 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: | Have & Be Co., Ltd. |
| NON-PROPRIETARY NAME: | ZINC OXIDE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE |
| SUBSTANCE NAME: | ZINC OXIDE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | CREAM |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2016-01-25 |
| END MARKETING DATE: | 0000-00-00 |
Dr.Jart Every Sun Day Sunscreen SPF 50 HUMAN OTC DRUG Details:
| Item Description | Dr.Jart Every Sun Day Sunscreen SPF 50 from Have & Be Co., Ltd. |
| LABELER NAME: | Have & Be Co., Ltd. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 6.33; 3.4; 2.25; 1.25(mg/50mL; mg/50mL; mg/50mL; mg/50mL) |
| START MARKETING DATE: | 2016-01-25 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 49404-130_3f42326a-6b16-31eb-e054-00144ff88e88 |
| PRODUCT NDC: | 49404-130 |
| APPLICATION NUMBER: | part352 |
Other ZINC OXIDE; OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE Pharmaceutical Manufacturers / Labelers:
