UltaSUNSCREEN SPF 45 (Prime Enterprises, Inc.)
Welcome to the PulseAid listing for the Ulta drug offered from Prime Enterprises, 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: | Prime Enterprises, Inc. |
| NON-PROPRIETARY NAME: | Octinoxate, Octisalate, Octocrylene, and Oxybenzone |
| SUBSTANCE NAME: | OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | LOTION |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2007-03-12 |
| END MARKETING DATE: | 0000-00-00 |
Ulta SUNSCREEN SPF 45 HUMAN OTC DRUG Details:
| Item Description | Ulta SUNSCREEN SPF 45 from Prime Enterprises, Inc. |
| LABELER NAME: | Prime Enterprises, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 71.25; 47.5; 76; 57(mg/mL; mg/mL; mg/mL; mg/mL) |
| START MARKETING DATE: | 2007-03-12 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 58443-0129_c1908946-0a8a-445f-9a80-47b843525dd1 |
| PRODUCT NDC: | 58443-0129 |
| APPLICATION NUMBER: | part352 |
Other OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE Pharmaceutical Manufacturers / Labelers:
