Eight Hour Cream Sun Defense for Face SPF 50 Sunscreen (Elizabeth Arden, Inc)
Welcome to the PulseAid listing for the Eight Hour Cream Sun Defense for Face SPF 50 Sunscreen 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: | Zinc Oxide |
| SUBSTANCE NAME: | ZINC OXIDE; OCTINOXATE; OCTISALATE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | LOTION |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2010-12-14 |
| END MARKETING DATE: | 0000-00-00 |
Eight Hour Cream Sun Defense for Face SPF 50 Sunscreen HUMAN OTC DRUG Details:
| Item Description | Eight Hour Cream Sun Defense for Face SPF 50 Sunscreen from Elizabeth Arden, Inc |
| LABELER NAME: | Elizabeth Arden, Inc |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 6.159; 3.922; 2.65(g/53g; g/53g; g/53g) |
| START MARKETING DATE: | 2010-12-14 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 67938-1094_3b8062cc-06a4-496e-8aa5-8fe2a940014d |
| PRODUCT NDC: | 67938-1094 |
| APPLICATION NUMBER: | part352 |
Other ZINC OXIDE; OCTINOXATE; OCTISALATE Pharmaceutical Manufacturers / Labelers:
