Pure Finish Mineral Tinted Moisturizer SPF 15 Deep (Elizabeth Arden, Inc)
Welcome to the PulseAid listing for the Pure Finish Mineral Tinted Moisturizer SPF 15 Deep drug offered from Elizabeth Arden, Inc. 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: | Elizabeth Arden, Inc |
| NON-PROPRIETARY NAME: | Octinoxate |
| SUBSTANCE NAME: | OCTINOXATE; TITANIUM DIOXIDE; OCTISALATE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | LOTION |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2010-07-26 |
| END MARKETING DATE: | 0000-00-00 |
Pure Finish Mineral Tinted Moisturizer SPF 15 Deep HUMAN OTC DRUG Details:
| Item Description | Pure Finish Mineral Tinted Moisturizer SPF 15 Deep from Elizabeth Arden, Inc |
| LABELER NAME: | Elizabeth Arden, Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 3; 2.15; 2(mL/50mL; mL/50mL; mL/50mL) |
| START MARKETING DATE: | 2010-07-26 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 67938-0909_644b092f-9fbf-466c-9471-0e3f2c42d0b5 |
| PRODUCT NDC: | 67938-0909 |
| APPLICATION NUMBER: | part352 |
Other OCTINOXATE; TITANIUM DIOXIDE; OCTISALATE Pharmaceutical Manufacturers / Labelers:
