Dr.Jart Every Sun Day Illuminating Sunscreen SPF 36 (Have & Be Co., Ltd.)
Welcome to the PulseAid listing for the Dr.Jart Every Sun Day Illuminating Sunscreen SPF 36 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: | OCTINOXATE, OCTISALATE, ENSULIZOLE, TITANIUM DIOXIDE, OCTOCRYLENE |
| SUBSTANCE NAME: | OCTINOXATE; OCTISALATE; ENSULIZOLE; TITANIUM DIOXIDE; OCTOCRYLENE |
| 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 Illuminating Sunscreen SPF 36 HUMAN OTC DRUG Details:
| Item Description | Dr.Jart Every Sun Day Illuminating Sunscreen SPF 36 from Have & Be Co., Ltd. |
| LABELER NAME: | Have & Be Co., Ltd. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 3.5; 2.25; 2; 1.15; .5(mg/50mL; mg/50mL; mg/50mL; mg/50mL; mg/50mL) |
| START MARKETING DATE: | 2016-01-25 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 49404-128_3f077d4c-577b-530a-e054-00144ff88e88 |
| PRODUCT NDC: | 49404-128 |
| APPLICATION NUMBER: | part352 |
Other OCTINOXATE; OCTISALATE; ENSULIZOLE; TITANIUM DIOXIDE; OCTOCRYLENE Pharmaceutical Manufacturers / Labelers:
