EGF UV SHIELD (Dermaesthetics Inc.)
Welcome to the PulseAid listing for the EGF UV SHIELD drug offered from Dermaesthetics 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: | Dermaesthetics Inc. |
| NON-PROPRIETARY NAME: | OCTINOXATE |
| SUBSTANCE NAME: | OCTINOXATE; OCTISALATE; ZINC OXIDE; TITANIUM DIOXIDE; AMILOXATE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | CREAM |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
| START MARKETING DATE: | 2013-06-26 |
| END MARKETING DATE: | 0000-00-00 |
EGF UV SHIELD HUMAN OTC DRUG Details:
| Item Description | EGF UV SHIELD from Dermaesthetics Inc. |
| LABELER NAME: | Dermaesthetics Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 7.5; 5; 4.9; 4.15; 2(g/60g; g/60g; g/60g; g/60g; g/60g) |
| START MARKETING DATE: | 2013-06-26 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 58831-1001_af3ce657-d6c9-4961-89f2-7eb15ecc63fa |
| PRODUCT NDC: | 58831-1001 |
| APPLICATION NUMBER: | part352 |
Other OCTINOXATE; OCTISALATE; ZINC OXIDE; TITANIUM DIOXIDE; AMILOXATE Pharmaceutical Manufacturers / Labelers:
